Organic electroluminescent materials and devices

ABSTRACT

A compound comprising a first ligand L A  of Formula I, 
     
       
         
         
             
             
         
       
     
     is disclosed. In Formula I, ring A is a 5- or 6-membered ring; K is selected from a direct bond and a linking group; two adjacent ones of X 1  to X 4  are CR and are fused to form a structure of Formula II, 
     
       
         
         
             
             
         
       
     
     each of X 1  to X 12  is CR or N; X is selected from a variety of linking groups; each R, R′, R″, and R A  is hydrogen or a substituent; L A  is coordinated to a metal M through the dashed lines in Formula I; and wherein (1) when X is CR′R″, X 5  is CR; and (2) when X is O, S, Se, or NR′, at least one of the following is true: (a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand; (b) at least one R comprises an electron withdrawing group; (c) at least two R A  is not hydrogen or deuterium; or (d) at least one R is selected from a specific group of structures.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application claims priority under 35 U.S.C. § 119(e) to U.S. Provisional Application No. 63/152,287, filed on Feb. 22, 2021, the entire contents of which are incorporated herein by reference.

FIELD

The present disclosure generally relates to organometallic compounds and formulations and their various uses including as emitters in devices such as organic light emitting diodes and related electronic devices.

BACKGROUND

Opto-electronic devices that make use of organic materials are becoming increasingly desirable for various reasons. Many of the materials used to make such devices are relatively inexpensive, so organic opto-electronic devices have the potential for cost advantages over inorganic devices. In addition, the inherent properties of organic materials, such as their flexibility, may make them well suited for particular applications such as fabrication on a flexible substrate. Examples of organic opto-electronic devices include organic light emitting diodes/devices (OLEDs), organic phototransistors, organic photovoltaic cells, and organic photodetectors. For OLEDs, the organic materials may have performance advantages over conventional materials.

OLEDs make use of thin organic films that emit light when voltage is applied across the device. OLEDs are becoming an increasingly interesting technology for use in applications such as flat panel displays, illumination, and backlighting.

One application for phosphorescent emissive molecules is a full color display. Industry standards for such a display call for pixels adapted to emit particular colors, referred to as “saturated” colors. In particular, these standards call for saturated red, green, and blue pixels. Alternatively, the OLED can be designed to emit white light. In conventional liquid crystal displays emission from a white backlight is filtered using absorption filters to produce red, green and blue emission. The same technique can also be used with OLEDs. The white OLED can be either a single emissive layer (EML) device or a stack structure. Color may be measured using CIE coordinates, which are well known to the art.

SUMMARY

In one aspect, the present disclosure provides a compound comprising a first ligand L_(A) of Formula I,

In Formula I:

ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

K is selected from the group consisting of a direct bond, O, S, NR′, CR′R″, and SiR′R″;

two adjacent ones of X¹ to X⁴ are CR and are fused to form a structure of Formula II,

where the dashed lines indicate direct bonds to ring B;

each of X¹ to X¹² independently represents CR or N, and each R can be same or different;

X is selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, Ge′RR″, SnR′R″, BR′, PR′, SbR′, and BiR′;

R^(A) represent mono to the maximum allowable substitution, or no substitution;

each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of the General Substituents as defined herein;

L_(A) is coordinated to a metal M through the indicated dashed lines;

the metal M has an atomic mass greater than 40;

the metal M can be coordinated to other ligands;

L_(A) may be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and

any two adjacent R, R′, R″, and R^(A) can be joined or fused to form a ring, with the proviso that

(1) when X is CR′R″, X⁵ is CR; and

(2) when X is O, S, Se, or NR′, at least one of the following is true:

(a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand;

(b) at least one R comprises an electron withdrawing group;

(c) at least two R^(A) is not hydrogen or deuterium; or

(d) at least one R is selected from the group consisting of the structures of the following LIST 1:

In another aspect, the present disclosure provides a formulation of the compound of the present disclosure.

In yet another aspect, the present disclosure provides an OLED having an organic layer comprising the compound of the present disclosure.

In yet another aspect, the present disclosure provides a consumer product comprising an OLED with an organic layer comprising the compound of the present disclosure.

BRIEF DESCRIPTION OF THE DRAWINGS

FIG. 1 shows an organic light emitting device.

FIG. 2 shows an inverted organic light emitting device that does not have a separate electron transport layer.

DETAILED DESCRIPTION A. Terminology

Unless otherwise specified, the below terms used herein are defined as follows:

As used herein, the term “organic” includes polymeric materials as well as small molecule organic materials that may be used to fabricate organic opto-electronic devices. “Small molecule” refers to any organic material that is not a polymer, and “small molecules” may actually be quite large. Small molecules may include repeat units in some circumstances. For example, using a long chain alkyl group as a substituent does not remove a molecule from the “small molecule” class. Small molecules may also be incorporated into polymers, for example as a pendent group on a polymer backbone or as a part of the backbone. Small molecules may also serve as the core moiety of a dendrimer, which consists of a series of chemical shells built on the core moiety. The core moiety of a dendrimer may be a fluorescent or phosphorescent small molecule emitter. A dendrimer may be a “small molecule,” and it is believed that all dendrimers currently used in the field of OLEDs are small molecules.

As used herein, “top” means furthest away from the substrate, while “bottom” means closest to the substrate. Where a first layer is described as “disposed over” a second layer, the first layer is disposed further away from substrate. There may be other layers between the first and second layer, unless it is specified that the first layer is “in contact with” the second layer. For example, a cathode may be described as “disposed over” an anode, even though there are various organic layers in between.

As used herein, “solution processable” means capable of being dissolved, dispersed, or transported in and/or deposited from a liquid medium, either in solution or suspension form.

A ligand may be referred to as “photoactive” when it is believed that the ligand directly contributes to the photoactive properties of an emissive material. A ligand may be referred to as “ancillary” when it is believed that the ligand does not contribute to the photoactive properties of an emissive material, although an ancillary ligand may alter the properties of a photoactive ligand.

As used herein, and as would be generally understood by one skilled in the art, a first “Highest Occupied Molecular Orbital” (HOMO) or “Lowest Unoccupied Molecular Orbital” (LUMO) energy level is “greater than” or “higher than” a second HOMO or LUMO energy level if the first energy level is closer to the vacuum energy level. Since ionization potentials (IP) are measured as a negative energy relative to a vacuum level, a higher HOMO energy level corresponds to an IP having a smaller absolute value (an IP that is less negative). Similarly, a higher LUMO energy level corresponds to an electron affinity (EA) having a smaller absolute value (an EA that is less negative). On a conventional energy level diagram, with the vacuum level at the top, the LUMO energy level of a material is higher than the HOMO energy level of the same material. A “higher” HOMO or LUMO energy level appears closer to the top of such a diagram than a “lower” HOMO or LUMO energy level.

As used herein, and as would be generally understood by one skilled in the art, a first work function is “greater than” or “higher than” a second work function if the first work function has a higher absolute value. Because work functions are generally measured as negative numbers relative to vacuum level, this means that a “higher” work function is more negative. On a conventional energy level diagram, with the vacuum level at the top, a “higher” work function is illustrated as further away from the vacuum level in the downward direction. Thus, the definitions of HOMO and LUMO energy levels follow a different convention than work functions.

The terms “halo,” “halogen,” and “halide” are used interchangeably and refer to fluorine, chlorine, bromine, and iodine.

The term “acyl” refers to a substituted carbonyl radical (C(O)—R_(s)).

The term “ester” refers to a substituted oxycarbonyl (—O—C(O)—R_(s) or —C(O)—O—R_(s)) radical.

The term “ether” refers to an —OR_(s) radical.

The terms “sulfanyl” or “thio-ether” are used interchangeably and refer to a —SR_(s) radical.

The term “selenyl” refers to a —SeR_(s) radical.

The term “sulfinyl” refers to a —S(O)—R_(s) radical.

The term “sulfonyl” refers to a —SO₂—R_(s) radical.

The term “phosphino” refers to a —P(R_(s))₃ radical, wherein each R_(s) can be same or different.

The term “silyl” refers to a —Si(R_(s))₃ radical, wherein each R_(s) can be same or different.

The term “germyl” refers to a —Ge(R_(s))₃ radical, wherein each R_(s) can be same or different.

The term “boryl” refers to a —B(R_(s))₂ radical or its Lewis adduct —B(R_(s))₃ radical, wherein R_(s) can be same or different.

In each of the above, R_(s) can be hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, and combination thereof. Preferred R_(s) is selected from the group consisting of alkyl, cycloalkyl, aryl, heteroaryl, and combination thereof.

The term “alkyl” refers to and includes both straight and branched chain alkyl radicals. Preferred alkyl groups are those containing from one to fifteen carbon atoms and includes methyl, ethyl, propyl, 1-methylethyl, butyl, 1-methylpropyl, 2-methylpropyl, pentyl, 1-methylbutyl, 2-methylbutyl, 3-methylbutyl, 1,1-dimethylpropyl, 1,2-dimethylpropyl, 2,2-dimethylpropyl, and the like. Additionally, the alkyl group may be optionally substituted.

The term “cycloalkyl” refers to and includes monocyclic, polycyclic, and spiro alkyl radicals. Preferred cycloalkyl groups are those containing 3 to 12 ring carbon atoms and includes cyclopropyl, cyclopentyl, cyclohexyl, bicyclo[3.1.1]heptyl, spiro[4.5]decyl, spiro[5.5]undecyl, adamantyl, and the like. Additionally, the cycloalkyl group may be optionally substituted.

The terms “heteroalkyl” or “heterocycloalkyl” refer to an alkyl or a cycloalkyl radical, respectively, having at least one carbon atom replaced by a heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si and Se, preferably, O, S or N. Additionally, the heteroalkyl or heterocycloalkyl group may be optionally substituted.

The term “alkenyl” refers to and includes both straight and branched chain alkene radicals. Alkenyl groups are essentially alkyl groups that include at least one carbon-carbon double bond in the alkyl chain. Cycloalkenyl groups are essentially cycloalkyl groups that include at least one carbon-carbon double bond in the cycloalkyl ring. The term “heteroalkenyl” as used herein refers to an alkenyl radical having at least one carbon atom replaced by a heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably, O, S, or N. Preferred alkenyl, cycloalkenyl, or heteroalkenyl groups are those containing two to fifteen carbon atoms. Additionally, the alkenyl, cycloalkenyl, or heteroalkenyl group may be optionally substituted.

The term “alkynyl” refers to and includes both straight and branched chain alkyne radicals. Alkynyl groups are essentially alkyl groups that include at least one carbon-carbon triple bond in the alkyl chain. Preferred alkynyl groups are those containing two to fifteen carbon atoms. Additionally, the alkynyl group may be optionally substituted.

The terms “aralkyl” or “arylalkyl” are used interchangeably and refer to an alkyl group that is substituted with an aryl group. Additionally, the aralkyl group may be optionally substituted.

The term “heterocyclic group” refers to and includes aromatic and non-aromatic cyclic radicals containing at least one heteroatom. Optionally the at least one heteroatom is selected from O, S, N, P, B, Si, and Se, preferably, O, S, or N. Heteroaromatic cyclic radicals may be used interchangeably with heteroaryl. Preferred hetero-non-aromatic cyclic groups are those containing 3 to 7 ring atoms which includes at least one hetero atom, and includes cyclic amines such as morpholino, piperidino, pyrrolidino, and the like, and cyclic ethers/thio-ethers, such as tetrahydrofuran, tetrahydropyran, tetrahydrothiophene, and the like. Additionally, the heterocyclic group may be optionally substituted.

The term “aryl” refers to and includes both single-ring aromatic hydrocarbyl groups and polycyclic aromatic ring systems. The polycyclic rings may have two or more rings in which two carbons are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is an aromatic hydrocarbyl group, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. Preferred aryl groups are those containing six to thirty carbon atoms, preferably six to twenty carbon atoms, more preferably six to twelve carbon atoms. Especially preferred is an aryl group having six carbons, ten carbons or twelve carbons. Suitable aryl groups include phenyl, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene, preferably phenyl, biphenyl, triphenyl, triphenylene, fluorene, and naphthalene. Additionally, the aryl group may be optionally substituted.

The term “heteroaryl” refers to and includes both single-ring aromatic groups and polycyclic aromatic ring systems that include at least one heteroatom. The heteroatoms include, but are not limited to O, S, N, P, B, Si, and Se. In many instances, O, S, or N are the preferred heteroatoms. Hetero-single ring aromatic systems are preferably single rings with 5 or 6 ring atoms, and the ring can have from one to six heteroatoms. The hetero-polycyclic ring systems can have two or more rings in which two atoms are common to two adjoining rings (the rings are “fused”) wherein at least one of the rings is a heteroaryl, e.g., the other rings can be cycloalkyls, cycloalkenyls, aryl, heterocycles, and/or heteroaryls. The hetero-polycyclic aromatic ring systems can have from one to six heteroatoms per ring of the polycyclic aromatic ring system. Preferred heteroaryl groups are those containing three to thirty carbon atoms, preferably three to twenty carbon atoms, more preferably three to twelve carbon atoms. Suitable heteroaryl groups include dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine, preferably dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, triazine, benzimidazole, 1,2-azaborine, 1,3-azaborine, 1,4-azaborine, borazine, and aza-analogs thereof. Additionally, the heteroaryl group may be optionally substituted.

Of the aryl and heteroaryl groups listed above, the groups of triphenylene, naphthalene, anthracene, dibenzothiophene, dibenzofuran, dibenzoselenophene, carbazole, indolocarbazole, imidazole, pyridine, pyrazine, pyrimidine, triazine, and benzimidazole, and the respective aza-analogs of each thereof are of particular interest.

The terms alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aralkyl, heterocyclic group, aryl, and heteroaryl, as used herein, are independently unsubstituted, or independently substituted, with one or more general substituents.

In many instances, the general substituents are selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, selenyl, sulfinyl, sulfonyl, phosphino, boryl, and combinations thereof.

In some instances, the preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, boryl, and combinations thereof.

In some instances, the more preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, alkoxy, aryloxy, amino, silyl, boryl, aryl, heteroaryl, sulfanyl, and combinations thereof.

In yet other instances, the most preferred general substituents are selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, aryl, heteroaryl, and combinations thereof.

The terms “substituted” and “substitution” refer to a substituent other than H that is bonded to the relevant position, e.g., a carbon or nitrogen. For example, when R¹ represents mono-substitution, then one R¹ must be other than H (i.e., a substitution). Similarly, when R¹ represents di-substitution, then two of R¹ must be other than H. Similarly, when R¹ represents zero or no substitution, R¹, for example, can be a hydrogen for available valencies of ring atoms, as in carbon atoms for benzene and the nitrogen atom in pyrrole, or simply represents nothing for ring atoms with fully filled valencies, e.g., the nitrogen atom in pyridine. The maximum number of substitutions possible in a ring structure will depend on the total number of available valencies in the ring atoms.

As used herein, “combinations thereof” indicates that one or more members of the applicable list are combined to form a known or chemically stable arrangement that one of ordinary skill in the art can envision from the applicable list. For example, an alkyl and deuterium can be combined to form a partial or fully deuterated alkyl group; a halogen and alkyl can be combined to form a halogenated alkyl substituent; and a halogen, alkyl, and aryl can be combined to form a halogenated arylalkyl. In one instance, the term substitution includes a combination of two to four of the listed groups. In another instance, the term substitution includes a combination of two to three groups. In yet another instance, the term substitution includes a combination of two groups. Preferred combinations of substituent groups are those that contain up to fifty atoms that are not hydrogen or deuterium, or those which include up to forty atoms that are not hydrogen or deuterium, or those that include up to thirty atoms that are not hydrogen or deuterium. In many instances, a preferred combination of substituent groups will include up to twenty atoms that are not hydrogen or deuterium.

The “aza” designation in the fragments described herein, i.e. aza-dibenzofuran, aza-dibenzothiophene, etc. means that one or more of the C—H groups in the respective aromatic ring can be replaced by a nitrogen atom, for example, and without any limitation, azatriphenylene encompasses both dibenzo[f,h]quinoxaline and dibenzo[f,h]quinoline. One of ordinary skill in the art can readily envision other nitrogen analogs of the aza-derivatives described above, and all such analogs are intended to be encompassed by the terms as set forth herein.

As used herein, “deuterium” refers to an isotope of hydrogen. Deuterated compounds can be readily prepared using methods known in the art. For example, U.S. Pat. No. 8,557,400, Patent Pub. No. WO 2006/095951, and U.S. Pat. Application Pub. No. US 2011/0037057, which are hereby incorporated by reference in their entireties, describe the making of deuterium-substituted organometallic complexes. Further reference is made to Ming Yan, et al., Tetrahedron 2015, 71, 1425-30 and Atzrodt et al., Angew. Chem. Int. Ed. (Reviews) 2007, 46, 7744-65, which are incorporated by reference in their entireties, describe the deuteration of the methylene hydrogens in benzyl amines and efficient pathways to replace aromatic ring hydrogens with deuterium, respectively.

It is to be understood that when a molecular fragment is described as being a substituent or otherwise attached to another moiety, its name may be written as if it were a fragment (e.g. phenyl, phenylene, naphthyl, dibenzofuryl) or as if it were the whole molecule (e.g. benzene, naphthalene, dibenzofuran). As used herein, these different ways of designating a substituent or attached fragment are considered to be equivalent.

In some instance, a pair of adjacent substituents can be optionally joined or fused into a ring. The preferred ring is a five, six, or seven-membered carbocyclic or heterocyclic ring, includes both instances where the portion of the ring formed by the pair of substituents is saturated and where the portion of the ring formed by the pair of substituents is unsaturated. As used herein, “adjacent” means that the two substituents involved can be on the same ring next to each other, or on two neighboring rings having the two closest available substitutable positions, such as 2, 2′ positions in a biphenyl, or 1, 8 position in a naphthalene, as long as they can form a stable fused ring system.

B. The Compounds of the Present Disclosure

In one aspect, the present disclosure provides a compound comprising a first ligand L_(A) of Formula I,

In Formula I:

ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

K is selected from the group consisting of a direct bond, O, S, NR′, CR′R″, and SiR′R″;

two adjacent ones of X¹ to X⁴ are C and are fused to form a structure of Formula II,

where the dashed lines indicate direct bonds to ring B;

each of X¹ to X¹² independently represents C, CR or N, and each R can be same or different;

X is selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, Ge′RR″, SnR′R″, BR′, PR′, SbR′, and BiR′;

R^(A) represent mono to the maximum allowable substitution, or no substitution;

each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of the general substituents as defined herein;

L_(A) is coordinated to a metal M through the indicated dashed lines;

the metal M has an atomic mass greater than 40;

the metal M can be coordinated to other ligands;

L_(A) may be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and

any two adjacent R, R′, R″, and R^(A) can be joined or fused to form a ring, with the proviso that that

(1) when X is CR′R″, X⁵ is CR; and

(2) when X is O, S, Se, or NR′, at least one of the following is true:

(a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand;

(b) at least one R comprises an electron withdrawing group;

(c) at least two R^(A) is not hydrogen or deuterium; or

(d) at least one R is selected from the group consisting of the structures of LIST 1 as defined herein.

In some embodiments, each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of the preferred general substituents as defined herein. In some embodiments, each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of the more preferred general substituents as defined herein. In some embodiments, each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of the most preferred general substituents as defined herein.

In some embodiments, K is a direct bond. In some embodiments, K is O. In some embodiments, K is S. In some embodiments, K is NR′. In some embodiments, K is CR′R″. In some embodiments, K is SiR′R″.

In some embodiments, X¹ and X² are CR and the Rs are fused to form a structure of Formula II.

In some embodiments, X² and X³ are CR and the Rs are fused to form a structure of Formula II.

In some embodiments, X³ and X⁴ are CR and the Rs are fused to form a structure of Formula II.

In some embodiments, L_(A) has the structure

and each of R^(A1), R^(A2), R^(A3), and R^(A4) is independently a hydrogen or a substituent selected from the group consisting of the general substituents as defined herein.

In some embodiments, at least one of R^(A1) to R^(A4) is other than hydrogen or deuterium. In some embodiments, at least two of R^(A1) to R^(A4) are other than hydrogen or deuterium.

In some embodiments, R^(A2) and R^(A4) are other than hydrogen or deuterium. In some embodiments, R^(A1) and R^(A3) are hydrogen or deuterium.

In some embodiments, X in Formula II is CR′R″, and X⁵ is CR.

In some embodiments, the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand.

In some embodiments, at least one R comprises an electron withdrawing group.

In some embodiments, at least one R is selected from the group consisting of the structures of LIST 1 as defined herein.

In some embodiments, at least one of X¹ to X¹² is N. In some embodiments, at least one of X¹ to X⁴ is N. In some embodiments, at least one of X⁵ to X¹² is N.

In some embodiments, each of X¹ to X¹² is CR. In some embodiments, each X¹ to X⁴ is CR. In some embodiments, each of X⁵ to X¹² is CR.

In some embodiments, X in Formula II is selected from the group consisting of SiR′R″, Ge′RR″, SnR′R″, BR′, PR′, SbR′, and BiR′.

In some embodiments, X in Formula II is selected from the group consisting of O, S, Se, and NR′.

In some embodiments, X in Formula II is selected from the group consisting of O, S, Se, and NR′; and (a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand.

In some embodiments, X in Formula II is selected from the group consisting of O, S, Se, and NR′, and (b) at least one R comprises an electron withdrawing group.

In some embodiments, X in Formula II is selected from the group consisting of O, S, Se, and NR′, and (c) at least two R^(A) is not hydrogen or deuterium.

In some embodiments, X in Formula II is selected from the group consisting of O, S, Se, and NR′, and (d) at least one R is selected from the group consisting of LIST 1 as defined herein.

In some embodiments, M is selected from the group consisting of Os, Ir, Pd, Pt, Cu, Ag, and Au.

In some embodiments, the ligand L_(A) has a structure of L_(Ai-m-X), where i is an integer from 1 to 4524, m is an integer from 1 to 184, and X in L_(Ai-m-X) is an integer from 1 to 4. In some such embodiments, wherein each of L_(Ai-1-X) to L_(Ai-184-X) has a structure in the following LIST 2:

where, when X in formula L_(Ai-m-X) is 1 it represents X in the above shown chemical structures being O, when X in L_(Ai-m-X) is 2 it represents X in the above shown chemical structures being S, when X in L_(Ai-m-X) is 3 it represents X in the above shown chemical structures being Se, when X in L_(Ai-m-X) is 4 it represents X in the above shown chemical structures being NR′;

where, for each i in L_(Ai-m-X), R^(E) and G are defined in the following LIST 3:

i R^(E) G i R^(E) G i R^(E) G i R^(E) G 1 R¹ G¹ 2 R¹ G² 3 R¹ G³ 4 R¹ G⁴ 5 R² G¹ 6 R² G² 7 R² G³ 8 R² G⁴ 9 R³ G¹ 10 R³ G² 11 R³ G³ 12 R³ G⁴ 13 R⁴ G¹ 14 R⁴ G² 15 R⁴ G³ 16 R⁴ G⁴ 17 R⁵ G¹ 18 R⁵ G² 19 R⁵ G³ 20 R⁵ G⁴ 21 R⁶ G¹ 22 R⁶ G² 23 R⁶ G³ 24 R⁶ G⁴ 25 R⁷ G¹ 26 R⁷ G² 27 R⁷ G³ 28 R⁷ G⁴ 29 R⁸ G¹ 30 R⁸ G² 31 R⁸ G³ 32 R⁸ G⁴ 33 R⁹ G¹ 34 R⁹ G² 35 R⁹ G³ 36 R⁹ G⁴ 37 R¹⁰ G¹ 38 R¹⁰ G² 39 R¹⁰ G³ 40 R¹⁰ G⁴ 41 R¹¹ G¹ 42 R¹¹ G² 43 R¹¹ G³ 44 R¹¹ G⁴ 45 R¹² G¹ 46 R¹² G² 47 R¹² G³ 48 R¹² G⁴ 49 R¹³ G¹ 50 R¹³ G² 51 R¹³ G³ 52 R¹³ G⁴ 53 R¹⁴ G¹ 54 R¹⁴ G² 55 R¹⁴ G³ 56 R¹⁴ G⁴ 57 R¹⁵ G¹ 58 R¹⁵ G² 59 R¹⁵ G³ 60 R¹⁵ G⁴ 61 R¹⁶ G¹ 62 R¹⁶ G² 63 R¹⁶ G³ 64 R¹⁶ G⁴ 65 R¹⁷ G¹ 66 R¹⁷ G² 67 R¹⁷ G³ 68 R¹⁷ G⁴ 69 R¹⁸ G¹ 70 R¹⁸ G² 71 R¹⁸ G³ 72 R¹⁸ G⁴ 73 R¹⁹ G¹ 74 R¹⁹ G² 75 R¹⁹ G³ 76 R¹⁹ G⁴ 77 R²⁰ G¹ 78 R²⁰ G² 79 R²⁰ G³ 80 R²⁰ G⁴ 81 R²¹ G¹ 82 R²¹ G² 83 R²¹ G³ 84 R²¹ G⁴ 85 R²² G¹ 86 R²² G² 87 R²² G³ 88 R²² G⁴ 89 R²³ G¹ 90 R²³ G² 91 R²³ G³ 92 R²³ G⁴ 93 R²⁴ G¹ 94 R²⁴ G² 95 R²⁴ G³ 96 R²⁴ G⁴ 97 R²⁵ G¹ 98 R²⁵ G² 99 R²⁵ G³ 100 R²⁵ G⁴ 101 R²⁶ G¹ 102 R²⁶ G² 103 R²⁶ G³ 104 R²⁶ G⁴ 105 R²⁷ G¹ 106 R²⁷ G² 107 R²⁷ G³ 108 R²⁷ G⁴ 109 R²⁸ G¹ 110 R²⁸ G² 111 R²⁸ G³ 112 R²⁸ G⁴ 113 R²⁹ G¹ 114 R²⁹ G² 115 R²⁹ G³ 116 R²⁹ G⁴ 117 R³⁰ G¹ 118 R³⁰ G² 119 R³⁰ G³ 120 R³⁰ G⁴ 121 R³¹ G¹ 122 R³¹ G² 123 R³¹ G³ 124 R³¹ G⁴ 125 R³² G¹ 126 R³² G² 127 R³² G³ 128 R³² G⁴ 129 R³³ G¹ 130 R³³ G² 131 R³³ G³ 132 R³³ G⁴ 133 R³⁴ G¹ 134 R³⁴ G² 135 R³⁴ G³ 136 R³⁴ G⁴ 137 R³⁵ G¹ 138 R³⁵ G² 139 R³⁵ G³ 140 R³⁵ G⁴ 141 R³⁶ G¹ 142 R³⁶ G² 143 R³⁶ G³ 144 R³⁶ G⁴ 145 R³⁷ G¹ 146 R³⁷ G² 147 R³⁷ G³ 148 R³⁷ G⁴ 149 R³⁸ G¹ 150 R³⁸ G² 151 R³⁸ G³ 152 R³⁸ G⁴ 153 R³⁹ G¹ 154 R³⁹ G² 155 R³⁹ G³ 156 R³⁹ G⁴ 157 R⁴⁰ G¹ 158 R⁴⁰ G² 159 R⁴⁰ G³ 160 R⁴⁰ G⁴ 161 R⁴¹ G¹ 162 R⁴¹ G² 163 R⁴¹ G³ 164 R⁴¹ G⁴ 165 R⁴² G¹ 166 R⁴² G² 167 R⁴² G³ 168 R⁴² G⁴ 169 R⁴³ G¹ 170 R⁴³ G² 171 R⁴³ G³ 172 R⁴³ G⁴ 173 R⁴⁴ G¹ 174 R⁴⁴ G² 175 R⁴⁴ G³ 176 R⁴⁴ G⁴ 177 R⁴⁵ G¹ 178 R⁴⁵ G² 179 R⁴⁵ G³ 180 R⁴⁵ G⁴ 181 R⁴⁶ G¹ 182 R⁴⁶ G² 183 R⁴⁶ G³ 184 R⁴⁶ G⁴ 185 R⁴⁷ G¹ 186 R⁴⁷ G² 187 R⁴⁷ G³ 188 R⁴⁷ G⁴ 189 R⁴⁸ G¹ 190 R⁴⁸ G² 191 R⁴⁸ G³ 192 R⁴⁸ G⁴ 193 R⁴⁹ G¹ 194 R⁴⁹ G² 195 R⁴⁹ G³ 196 R⁴⁹ G⁴ 197 R⁵⁰ G¹ 198 R⁵⁰ G² 199 R⁵⁰ G³ 200 R⁵⁰ G⁴ 201 R⁵¹ G¹ 202 R⁵¹ G² 203 R⁵¹ G³ 204 R⁵¹ G⁴ 205 R⁵² G¹ 206 R⁵² G² 207 R⁵² G³ 208 R⁵² G⁴ 209 R⁵³ G¹ 210 R⁵³ G² 211 R⁵³ G³ 212 R⁵³ G⁴ 213 R⁵⁴ G¹ 214 R⁵⁴ G² 215 R⁵⁴ G³ 216 R⁵⁴ G⁴ 217 R⁵⁵ G¹ 218 R⁵⁵ G² 219 R⁵⁵ G³ 220 R⁵⁵ G⁴ 221 R⁵⁶ G¹ 222 R⁵⁶ G² 223 R⁵⁶ G³ 224 R⁵⁶ G⁴ 225 R⁵⁷ G¹ 226 R⁵⁷ G² 227 R⁵⁷ G³ 228 R⁵⁷ G⁴ 229 R⁵⁸ G¹ 230 R⁵⁸ G² 231 R⁵⁸ G³ 232 R⁵⁸ G⁴ 233 R⁵⁹ G¹ 234 R⁵⁹ G² 235 R⁵⁹ G³ 236 R⁵⁹ G⁴ 237 R⁶⁰ G¹ 238 R⁶⁰ G² 239 R⁶⁰ G³ 240 R⁶⁰ G⁴ 241 R⁶¹ G¹ 242 R⁶¹ G² 243 R⁶¹ G³ 244 R⁶¹ G⁴ 245 R⁶² G¹ 246 R⁶² G² 247 R⁶² G³ 248 R⁶² G⁴ 249 R⁶³ G¹ 250 R⁶³ G² 251 R⁶³ G³ 252 R⁶³ G⁴ 253 R⁶⁴ G¹ 254 R⁶⁴ G² 255 R⁶⁴ G³ 256 R⁶⁴ G⁴ 257 R⁶⁵ G¹ 258 R⁶⁵ G² 259 R⁶⁵ G³ 260 R⁶⁵ G⁴ 261 R⁶⁶ G¹ 262 R⁶⁶ G² 263 R⁶⁶ G³ 264 R⁶⁶ G⁴ 265 R⁶⁷ G¹ 266 R⁶⁷ G² 267 R⁶⁷ G³ 268 R⁶⁷ G⁴ 269 R⁶⁸ G¹ 270 R⁶⁸ G² 271 R⁶⁸ G³ 272 R⁶⁸ G⁴ 273 R⁶⁹ G¹ 274 R⁶⁹ G² 275 R⁶⁹ G³ 276 R⁶⁹ G⁴ 277 R⁷⁰ G¹ 278 R⁷⁰ G² 279 R⁷⁰ G³ 280 R⁷⁰ G⁴ 281 R⁷¹ G¹ 282 R⁷¹ G² 283 R⁷¹ G³ 284 R⁷¹ G⁴ 285 R⁷² G¹ 286 R⁷² G² 287 R⁷² G³ 288 R⁷² G⁴ 289 R⁷³ G¹ 290 R⁷³ G² 291 R⁷³ G³ 292 R⁷³ G⁴ 293 R⁷⁴ G¹ 294 R⁷⁴ G² 295 R⁷⁴ G³ 296 R⁷⁴ G⁴ 297 R⁷⁵ G¹ 298 R⁷⁵ G² 299 R⁷⁵ G³ 300 R⁷⁵ G⁴ 301 R⁷⁶ G¹ 302 R⁷⁶ G² 303 R⁷⁶ G³ 304 R⁷⁶ G⁴ 305 R⁷⁷ G¹ 306 R⁷⁷ G² 307 R⁷⁷ G³ 308 R⁷⁷ G⁴ 309 R⁷⁸ G¹ 310 R⁷⁸ G² 311 R⁷⁸ G³ 312 R⁷⁸ G⁴ 313 R⁷⁹ G¹ 314 R⁷⁹ G² 315 R⁷⁹ G³ 316 R⁷⁹ G⁴ 317 R⁸⁰ G¹ 318 R⁸⁰ G² 319 R⁸⁰ G³ 320 R⁸⁰ G⁴ 321 R⁸¹ G¹ 322 R⁸¹ G² 323 R⁸¹ G³ 324 R⁸¹ G⁴ 325 R⁸² G¹ 326 R⁸² G² 327 R⁸² G³ 328 R⁸² G⁴ 329 R⁸³ G¹ 330 R⁸³ G² 331 R⁸³ G³ 332 R⁸³ G⁴ 333 R⁸⁴ G¹ 334 R⁸⁴ G² 335 R⁸⁴ G³ 336 R⁸⁴ G⁴ 337 R⁸⁵ G¹ 338 R⁸⁵ G² 339 R⁸⁵ G³ 340 R⁸⁵ G⁴ 341 R⁸⁶ G¹ 342 R⁸⁶ G² 343 R⁸⁶ G³ 344 R⁸⁶ G⁴ 345 R⁸⁷ G¹ 346 R⁸⁷ G² 347 R⁸⁷ G³ 348 R⁸⁷ G⁴ 349 R¹ G⁵ 350 R¹ G⁶ 351 R¹ G⁷ 352 R¹ G⁸ 353 R² G⁵ 354 R² G⁶ 355 R² G⁷ 356 R² G⁸ 357 R³ G⁵ 358 R³ G⁶ 359 R³ G⁷ 360 R³ G⁸ 361 R⁴ G⁵ 362 R⁴ G⁶ 363 R⁴ G⁷ 364 R⁴ G⁸ 365 R⁵ G⁵ 366 R⁵ G⁶ 367 R⁵ G⁷ 368 R⁵ G⁸ 369 R⁶ G⁵ 370 R⁶ G⁶ 371 R⁶ G⁷ 372 R⁶ G⁸ 373 R⁷ G⁵ 374 R⁷ G⁶ 375 R⁷ G⁷ 376 R⁷ G⁸ 377 R⁸ G⁵ 378 R⁸ G⁶ 379 R⁸ G⁷ 380 R⁸ G⁸ 381 R⁹ G⁵ 382 R⁹ G⁶ 383 R⁹ G⁷ 384 R⁹ G⁸ 385 R¹⁰ G⁵ 386 R¹⁰ G⁶ 387 R¹⁰ G⁷ 388 R¹⁰ G⁸ 389 R¹¹ G⁵ 390 R¹¹ G⁶ 391 R¹¹ G⁷ 392 R¹¹ G⁸ 393 R¹² G⁵ 394 R¹² G⁶ 395 R¹² G⁷ 396 R¹² G⁸ 397 R¹³ G⁵ 398 R¹³ G⁶ 399 R¹³ G⁷ 400 R¹³ G⁸ 401 R¹⁴ G⁵ 402 R¹⁴ G⁶ 403 R¹⁴ G⁷ 404 R¹⁴ G⁸ 405 R¹⁵ G⁵ 406 R¹⁵ G⁶ 407 R¹⁵ G⁷ 408 R¹⁵ G⁸ 409 R¹⁶ G⁵ 410 R¹⁶ G⁶ 411 R¹⁶ G⁷ 412 R¹⁶ G⁸ 413 R¹⁷ G⁵ 414 R¹⁷ G⁶ 415 R¹⁷ G⁷ 416 R¹⁷ G⁸ 417 R¹⁸ G⁵ 418 R¹⁸ G⁶ 419 R¹⁸ G⁷ 420 R¹⁸ G⁸ 421 R¹⁹ G⁵ 422 R¹⁹ G⁶ 423 R¹⁹ G⁷ 424 R¹⁹ G⁸ 425 R²⁰ G⁵ 426 R²⁰ G⁶ 427 R²⁰ G⁷ 428 R²⁰ G⁸ 429 R²¹ G⁵ 430 R²¹ G⁶ 431 R²¹ G⁷ 432 R²¹ G⁸ 433 R²² G⁵ 434 R²² G⁶ 435 R²² G⁷ 436 R²² G⁸ 437 R²³ G⁵ 438 R²³ G⁶ 439 R²³ G⁷ 440 R²³ G⁸ 441 R²⁴ G⁵ 442 R²⁴ G⁶ 443 R²⁴ G⁷ 444 R²⁴ G⁸ 445 R²⁵ G⁵ 446 R²⁵ G⁶ 447 R²⁵ G⁷ 448 R²⁵ G⁸ 449 R²⁶ G⁵ 450 R²⁶ G⁶ 451 R²⁶ G⁷ 452 R²⁶ G⁸ 453 R²⁷ G⁵ 454 R²⁷ G⁶ 455 R²⁷ G⁷ 456 R²⁷ G⁸ 457 R²⁸ G⁵ 458 R²⁸ G⁶ 459 R²⁸ G⁷ 460 R²⁸ G⁸ 461 R²⁹ G⁵ 462 R²⁹ G⁶ 463 R²⁹ G⁷ 464 R²⁹ G⁸ 465 R³⁰ G⁵ 466 R³⁰ G⁶ 467 R³⁰ G⁷ 468 R³⁰ G⁸ 469 R³¹ G⁵ 470 R³¹ G⁶ 471 R³¹ G⁷ 472 R³¹ G⁸ 473 R³² G⁵ 474 R³² G⁶ 475 R³² G⁷ 476 R³² G⁸ 477 R³³ G⁵ 478 R³³ G⁶ 479 R³³ G⁷ 480 R³³ G⁸ 481 R³⁴ G⁵ 482 R³⁴ G⁶ 483 R³⁴ G⁷ 484 R³⁴ G⁸ 485 R³⁵ G⁵ 486 R³⁵ G⁶ 487 R³⁵ G⁷ 488 R³⁵ G⁸ 489 R³⁶ G⁵ 490 R³⁶ G⁶ 491 R³⁶ G⁷ 492 R³⁶ G⁸ 493 R³⁷ G⁵ 494 R³⁷ G⁶ 495 R³⁷ G⁷ 496 R³⁷ G⁸ 497 R³⁸ G⁵ 498 R³⁸ G⁶ 499 R³⁸ G⁷ 500 R³⁸ G⁸ 501 R³⁹ G⁵ 502 R³⁹ G⁶ 503 R³⁹ G⁷ 504 R³⁹ G⁸ 505 R⁴⁰ G⁵ 506 R⁴⁰ G⁶ 507 R⁴⁰ G⁷ 508 R⁴⁰ G⁸ 509 R⁴¹ G⁵ 510 R⁴¹ G⁶ 511 R⁴¹ G⁷ 512 R⁴¹ G⁸ 513 R⁴² G⁵ 514 R⁴² G⁶ 515 R⁴² G⁷ 516 R⁴² G⁸ 517 R⁴³ G⁵ 518 R⁴³ G⁶ 519 R⁴³ G⁷ 520 R⁴³ G⁸ 521 R⁴⁴ G⁵ 522 R⁴⁴ G⁶ 523 R⁴⁴ G⁷ 524 R⁴⁴ G⁸ 525 R⁴⁵ G⁵ 526 R⁴⁵ G⁶ 527 R⁴⁵ G⁷ 528 R⁴⁵ G⁸ 529 R⁴⁶ G⁵ 530 R⁴⁶ G⁶ 531 R⁴⁶ G⁷ 532 R⁴⁶ G⁸ 533 R⁴⁷ G⁵ 534 R⁴⁷ G⁶ 535 R⁴⁷ G⁷ 536 R⁴⁷ G⁸ 537 R⁴⁸ G⁵ 538 R⁴⁸ G⁶ 539 R⁴⁸ G⁷ 540 R⁴⁸ G⁸ 541 R⁴⁹ G⁵ 542 R⁴⁹ G⁶ 543 R⁴⁹ G⁷ 544 R⁴⁹ G⁸ 545 R⁵⁰ G⁵ 546 R⁵⁰ G⁶ 547 R⁵⁰ G⁷ 548 R⁵⁰ G⁸ 549 R⁵¹ G⁵ 550 R⁵¹ G⁶ 551 R⁵¹ G⁷ 552 R⁵¹ G⁸ 553 R⁵² G⁵ 554 R⁵² G⁶ 555 R⁵² G⁷ 556 R⁵² G⁸ 557 R⁵³ G⁵ 558 R⁵³ G⁶ 559 R⁵³ G⁷ 560 R⁵³ G⁸ 561 R⁵⁴ G⁵ 562 R⁵⁴ G⁶ 563 R⁵⁴ G⁷ 564 R⁵⁴ G⁸ 565 R⁵⁵ G⁵ 566 R⁵⁵ G⁶ 567 R⁵⁵ G⁷ 568 R⁵⁵ G⁸ 569 R⁵⁶ G⁵ 570 R⁵⁶ G⁶ 571 R⁵⁶ G⁷ 572 R⁵⁶ G⁸ 573 R⁵⁷ G⁵ 574 R⁵⁷ G⁶ 575 R⁵⁷ G⁷ 576 R⁵⁷ G⁸ 577 R⁵⁸ G⁵ 578 R⁵⁸ G⁶ 579 R⁵⁸ G⁷ 580 R⁵⁸ G⁸ 581 R⁵⁹ G⁵ 582 R⁵⁹ G⁶ 583 R⁵⁹ G⁷ 584 R⁵⁹ G⁸ 585 R⁶⁰ G⁵ 586 R⁶⁰ G⁶ 587 R⁶⁰ G⁷ 588 R⁶⁰ G⁸ 589 R⁶¹ G⁵ 590 R⁶¹ G⁶ 591 R⁶¹ G⁷ 592 R⁶¹ G⁸ 593 R⁶² G⁵ 594 R⁶² G⁶ 595 R⁶² G⁷ 596 R⁶² G⁸ 597 R⁶³ G⁵ 598 R⁶³ G⁶ 599 R⁶³ G⁷ 600 R⁶³ G⁸ 601 R⁶⁴ G⁵ 602 R⁶⁴ G⁶ 603 R⁶⁴ G⁷ 604 R⁶⁴ G⁸ 605 R⁶⁵ G⁵ 606 R⁶⁵ G⁶ 607 R⁶⁵ G⁷ 608 R⁶⁵ G⁸ 609 R⁶⁶ G⁵ 610 R⁶⁶ G⁶ 611 R⁶⁶ G⁷ 612 R⁶⁶ G⁸ 613 R⁶⁷ G⁵ 614 R⁶⁷ G⁶ 615 R⁶⁷ G⁷ 616 R⁶⁷ G⁸ 617 R⁶⁸ G⁵ 618 R⁶⁸ G⁶ 619 R⁶⁸ G⁷ 620 R⁶⁸ G⁸ 621 R⁶⁹ G⁵ 622 R⁶⁹ G⁶ 623 R⁶⁹ G⁷ 624 R⁶⁹ G⁸ 625 R⁷⁰ G⁵ 626 R⁷⁰ G⁶ 627 R⁷⁰ G⁷ 628 R⁷⁰ G⁸ 629 R⁷¹ G⁵ 630 R⁷¹ G⁶ 631 R⁷¹ G⁷ 632 R⁷¹ G⁸ 633 R⁷² G⁵ 634 R⁷² G⁶ 635 R⁷² G⁷ 636 R⁷² G⁸ 637 R⁷³ G⁵ 638 R⁷³ G⁶ 639 R⁷³ G⁷ 640 R⁷³ G⁸ 641 R⁷⁴ G⁵ 642 R⁷⁴ G⁶ 643 R⁷⁴ G⁷ 644 R⁷⁴ G⁸ 645 R⁷⁵ G⁵ 646 R⁷⁵ G⁶ 647 R⁷⁵ G⁷ 648 R⁷⁵ G⁸ 649 R⁷⁶ G⁵ 650 R⁷⁶ G⁶ 651 R⁷⁶ G⁷ 652 R⁷⁶ G⁸ 653 R⁷⁷ G⁵ 654 R⁷⁷ G⁶ 655 R⁷⁷ G⁷ 656 R⁷⁷ G⁸ 657 R⁷⁸ G⁵ 658 R⁷⁸ G⁶ 659 R⁷⁸ G⁷ 660 R⁷⁸ G⁸ 661 R⁷⁹ G⁵ 662 R⁷⁹ G⁶ 663 R⁷⁹ G⁷ 664 R⁷⁹ G⁸ 665 R⁸⁰ G⁵ 666 R⁸⁰ G⁶ 667 R⁸⁰ G⁷ 668 R⁸⁰ G⁸ 669 R⁸¹ G⁵ 670 R⁸¹ G⁶ 671 R⁸¹ G⁷ 672 R⁸¹ G⁸ 673 R⁸² G⁵ 674 R⁸² G⁶ 675 R⁸² G⁷ 676 R⁸² G⁸ 677 R⁸³ G⁵ 678 R⁸³ G⁶ 679 R⁸³ G⁷ 680 R⁸³ G⁸ 681 R⁸⁴ G⁵ 682 R⁸⁴ G⁶ 683 R⁸⁴ G⁷ 684 R⁸⁴ G⁸ 685 R⁸⁵ G⁵ 686 R⁸⁵ G⁶ 687 R⁸⁵ G⁷ 688 R⁸⁵ G⁸ 689 R⁸⁶ G⁵ 690 R⁸⁶ G⁶ 691 R⁸⁶ G⁷ 692 R⁸⁶ G⁸ 693 R⁸⁷ G⁵ 694 R⁸⁷ G⁶ 695 R⁸⁷ G⁷ 696 R⁸⁷ G⁸ 697 R¹ G⁹ 698 R¹ G¹⁰ 699 R¹ G¹¹ 700 R¹ G¹² 701 R² G⁹ 702 R² G¹⁰ 703 R² G¹¹ 704 R² G¹² 705 R³ G⁹ 706 R³ G¹⁰ 707 R³ G¹¹ 708 R³ G¹² 709 R⁴ G⁹ 710 R⁴ G¹⁰ 711 R⁴ G¹¹ 712 R⁴ G¹² 713 R⁵ G⁹ 714 R⁵ G¹⁰ 715 R⁵ G¹¹ 716 R⁵ G¹² 717 R⁶ G⁹ 718 R⁶ G¹⁰ 719 R⁶ G¹¹ 720 R⁶ G¹² 721 R⁷ G⁹ 722 R⁷ G¹⁰ 723 R⁷ G¹¹ 724 R⁷ G¹² 725 R⁸ G⁹ 726 R⁸ G¹⁰ 727 R⁸ G¹¹ 728 R⁸ G¹² 729 R⁹ G⁹ 730 R⁹ G¹⁰ 731 R⁹ G¹¹ 732 R⁹ G¹² 733 R¹⁰ G⁹ 734 R¹⁰ G¹⁰ 735 R¹⁰ G¹¹ 736 R¹⁰ G¹² 737 R¹¹ G⁹ 738 R¹¹ G¹⁰ 739 R¹¹ G¹¹ 740 R¹¹ G¹² 741 R¹² G⁹ 742 R¹² G¹⁰ 743 R¹² G¹¹ 744 R¹² G¹² 745 R¹³ G⁹ 746 R¹³ G¹⁰ 747 R¹³ G¹¹ 748 R¹³ G¹² 749 R¹⁴ G⁹ 750 R¹⁴ G¹⁰ 751 R¹⁴ G¹¹ 752 R¹⁴ G¹² 753 R¹⁵ G⁹ 754 R¹⁵ G¹⁰ 755 R¹⁵ G¹¹ 756 R¹⁵ G¹² 757 R¹⁶ G⁹ 758 R¹⁶ G¹⁰ 759 R¹⁶ G¹¹ 760 R¹⁶ G¹² 761 R¹⁷ G⁹ 762 R¹⁷ G¹⁰ 763 R¹⁷ G¹¹ 764 R¹⁷ G¹² 765 R¹⁸ G⁹ 766 R¹⁸ G¹⁰ 767 R¹⁸ G¹¹ 768 R¹⁸ G¹² 769 R¹⁹ G⁹ 770 R¹⁹ G¹⁰ 771 R¹⁹ G¹¹ 772 R¹⁹ G¹² 773 R²⁰ G⁹ 774 R²⁰ G¹⁰ 775 R²⁰ G¹¹ 776 R²⁰ G¹² 777 R²¹ G⁹ 778 R²¹ G¹⁰ 779 R²¹ G¹¹ 780 R²¹ G¹² 781 R²² G⁹ 782 R²² G¹⁰ 783 R²² G¹¹ 784 R²² G¹² 785 R²³ G⁹ 786 R²³ G¹⁰ 787 R²³ G¹¹ 788 R²³ G¹² 789 R²⁴ G⁹ 790 R²⁴ G¹⁰ 791 R²⁴ G¹¹ 792 R²⁴ G¹² 793 R²⁵ G⁹ 794 R²⁵ G¹⁰ 795 R²⁵ G¹¹ 796 R²⁵ G¹² 797 R²⁶ G⁹ 798 R²⁶ G¹⁰ 799 R²⁶ G¹¹ 800 R²⁶ G¹² 801 R²⁷ G⁹ 802 R²⁷ G¹⁰ 803 R²⁷ G¹¹ 804 R²⁷ G¹² 805 R²⁸ G⁹ 806 R²⁸ G¹⁰ 807 R²⁸ G¹¹ 808 R²⁸ G¹² 809 R²⁹ G⁹ 810 R²⁹ G¹⁰ 811 R²⁹ G¹¹ 812 R²⁹ G¹² 813 R³⁰ G⁹ 814 R³⁰ G¹⁰ 815 R³⁰ G¹¹ 816 R³⁰ G¹² 817 R³¹ G⁹ 818 R³¹ G¹⁰ 819 R³¹ G¹¹ 820 R³¹ G¹² 821 R³² G⁹ 822 R³² G¹⁰ 823 R³² G¹¹ 824 R³² G¹² 825 R³³ G⁹ 826 R³³ G¹⁰ 827 R³³ G¹¹ 828 R³³ G¹² 829 R³⁴ G⁹ 830 R³⁴ G¹⁰ 831 R³⁴ G¹¹ 832 R³⁴ G¹² 833 R³⁵ G⁹ 834 R³⁵ G¹⁰ 835 R³⁵ G¹¹ 836 R³⁵ G¹² 837 R³⁶ G⁹ 838 R³⁶ G¹⁰ 839 R³⁶ G¹¹ 840 R³⁶ G¹² 841 R³⁷ G⁹ 842 R³⁷ G¹⁰ 843 R³⁷ G¹¹ 844 R³⁷ G¹² 845 R³⁸ G⁹ 846 R³⁸ G¹⁰ 847 R³⁸ G¹¹ 848 R³⁸ G¹² 849 R³⁹ G⁹ 850 R³⁹ G¹⁰ 851 R³⁹ G¹¹ 852 R³⁹ G¹² 853 R⁴⁰ G⁹ 854 R⁴⁰ G¹⁰ 855 R⁴⁰ G¹¹ 856 R⁴⁰ G¹² 857 R⁴¹ G⁹ 858 R⁴¹ G¹⁰ 859 R⁴¹ G¹¹ 860 R⁴¹ G¹² 861 R⁴² G⁹ 862 R⁴² G¹⁰ 863 R⁴² G¹¹ 864 R⁴² G¹² 865 R⁴³ G⁹ 866 R⁴³ G¹⁰ 867 R⁴³ G¹¹ 868 R⁴³ G¹² 869 R⁴⁴ G⁹ 870 R⁴⁴ G¹⁰ 871 R⁴⁴ G¹¹ 872 R⁴⁴ G¹² 873 R⁴⁵ G⁹ 874 R⁴⁵ G¹⁰ 875 R⁴⁵ G¹¹ 876 R⁴⁵ G¹² 877 R⁴⁶ G⁹ 878 R⁴⁶ G¹⁰ 879 R⁴⁶ G¹¹ 880 R⁴⁶ G¹² 881 R⁴⁷ G⁹ 882 R⁴⁷ G¹⁰ 883 R⁴⁷ G¹¹ 884 R⁴⁷ G¹² 885 R⁴⁸ G⁹ 886 R⁴⁸ G¹⁰ 887 R⁴⁸ G¹¹ 888 R⁴⁸ G¹² 889 R⁴⁹ G⁹ 890 R⁴⁹ G¹⁰ 891 R⁴⁹ G¹¹ 892 R⁴⁹ G¹² 893 R⁵⁰ G⁹ 894 R⁵⁰ G¹⁰ 895 R⁵⁰ G¹¹ 896 R⁵⁰ G¹² 897 R⁵¹ G⁹ 898 R⁵¹ G¹⁰ 899 R⁵¹ G¹¹ 900 R⁵¹ G¹² 901 R⁵² G⁹ 902 R⁵² G¹⁰ 903 R⁵² G¹¹ 904 R⁵² G¹² 905 R⁵³ G⁹ 906 R⁵³ G¹⁰ 907 R⁵³ G¹¹ 908 R⁵³ G¹² 909 R⁵⁴ G⁹ 910 R⁵⁴ G¹⁰ 911 R⁵⁴ G¹¹ 912 R⁵⁴ G¹² 913 R⁵⁵ G⁹ 914 R⁵⁵ G¹⁰ 915 R⁵⁵ G¹¹ 916 R⁵⁵ G¹² 917 R⁵⁶ G⁹ 918 R⁵⁶ G¹⁰ 919 R⁵⁶ G¹¹ 920 R⁵⁶ G¹² 921 R⁵⁷ G⁹ 922 R⁵⁷ G¹⁰ 923 R⁵⁷ G¹¹ 924 R⁵⁷ G¹² 925 R⁵⁸ G⁹ 926 R⁵⁸ G¹⁰ 927 R⁵⁸ G¹¹ 928 R⁵⁸ G¹² 929 R⁵⁹ G⁹ 930 R⁵⁹ G¹⁰ 931 R⁵⁹ G¹¹ 932 R⁵⁹ G¹² 933 R⁶⁰ G⁹ 934 R⁶⁰ G¹⁰ 935 R⁶⁰ G¹¹ 936 R⁶⁰ G¹² 937 R⁶¹ G⁹ 938 R⁶¹ G¹⁰ 939 R⁶¹ G¹¹ 940 R⁶¹ G¹² 941 R⁶² G⁹ 942 R⁶² G¹⁰ 943 R⁶² G¹¹ 944 R⁶² G¹² 945 R⁶³ G⁹ 946 R⁶³ G¹⁰ 947 R⁶³ G¹¹ 948 R⁶³ G¹² 949 R⁶⁴ G⁹ 950 R⁶⁴ G¹⁰ 951 R⁶⁴ G¹¹ 952 R⁶⁴ G¹² 953 R⁶⁵ G⁹ 954 R⁶⁵ G¹⁰ 955 R⁶⁵ G¹¹ 956 R⁶⁵ G¹² 957 R⁶⁶ G⁹ 958 R⁶⁶ G¹⁰ 959 R⁶⁶ G¹¹ 960 R⁶⁶ G¹² 961 R⁶⁷ G⁹ 962 R⁶⁷ G¹⁰ 963 R⁶⁷ G¹¹ 964 R⁶⁷ G¹² 965 R⁶⁸ G⁹ 966 R⁶⁸ G¹⁰ 967 R⁶⁸ G¹¹ 968 R⁶⁸ G¹² 969 R⁶⁹ G⁹ 970 R⁶⁹ G¹⁰ 971 R⁶⁹ G¹¹ 972 R⁶⁹ G¹² 973 R⁷⁰ G⁹ 974 R⁷⁰ G¹⁰ 975 R⁷⁰ G¹¹ 976 R⁷⁰ G¹² 977 R⁷¹ G⁹ 978 R⁷¹ G¹⁰ 979 R⁷¹ G¹¹ 980 R⁷¹ G¹² 981 R⁷² G⁹ 982 R⁷² G¹⁰ 983 R⁷² G¹¹ 984 R⁷² G¹² 985 R⁷³ G⁹ 986 R⁷³ G¹⁰ 987 R⁷³ G¹¹ 988 R⁷³ G¹² 989 R⁷⁴ G⁹ 990 R⁷⁴ G¹⁰ 991 R⁷⁴ G¹¹ 992 R⁷⁴ G¹² 993 R⁷⁵ G⁹ 994 R⁷⁵ G¹⁰ 995 R⁷⁵ G¹¹ 996 R⁷⁵ G¹² 997 R⁷⁶ G⁹ 998 R⁷⁶ G¹⁰ 999 R⁷⁶ G¹¹ 1000 R⁷⁶ G¹² 1001 R⁷⁷ G⁹ 1002 R⁷⁷ G¹⁰ 1003 R⁷⁷ G¹¹ 1004 R⁷⁷ G¹² 1005 R⁷⁸ G⁹ 1006 R⁷⁸ G¹⁰ 1007 R⁷⁸ G¹¹ 1008 R⁷⁸ G¹² 1009 R⁷⁹ G⁹ 1010 R⁷⁹ G¹⁰ 1011 R⁷⁹ G¹¹ 1012 R⁷⁹ G¹² 1013 R⁸⁰ G⁹ 1014 R⁸⁰ G¹⁰ 1015 R⁸⁰ G¹¹ 1016 R⁸⁰ G¹² 1017 R⁸¹ G⁹ 1018 R⁸¹ G¹⁰ 1019 R⁸¹ G¹¹ 1020 R⁸¹ G¹² 1021 R⁸² G⁹ 1022 R⁸² G¹⁰ 1023 R⁸² G¹¹ 1024 R⁸² G¹² 1025 R⁸³ G⁹ 1026 R⁸³ G¹⁰ 1027 R⁸³ G¹¹ 1028 R⁸³ G¹² 1029 R⁸⁴ G⁹ 1030 R⁸⁴ G¹⁰ 1031 R⁸⁴ G¹¹ 1032 R⁸⁴ G¹² 1033 R⁸⁵ G⁹ 1034 R⁸⁵ G¹⁰ 1035 R⁸⁵ G¹¹ 1036 R⁸⁵ G¹² 1037 R⁸⁶ G⁹ 1038 R⁸⁶ G¹⁰ 1039 R⁸⁶ G¹¹ 1040 R⁸⁶ G¹² 1041 R⁸⁷ G⁹ 1042 R⁸⁷ G¹⁰ 1043 R⁸⁷ G¹¹ 1044 R⁸⁷ G¹² 1045 R¹ G¹³ 1046 R¹ G¹⁴ 1047 R¹ G¹⁵ 1048 R¹ G¹⁶ 1049 R² G¹³ 1050 R² G¹⁴ 1051 R² G¹⁵ 1052 R² G¹⁶ 1053 R³ G¹³ 1054 R³ G¹⁴ 1055 R³ G¹⁵ 1056 R³ G¹⁶ 1057 R⁴ G¹³ 1058 R⁴ G¹⁴ 1059 R⁴ G¹⁵ 1060 R⁴ G¹⁶ 1061 R⁵ G¹³ 1062 R⁵ G¹⁴ 1063 R⁵ G¹⁵ 1064 R⁵ G¹⁶ 1065 R⁶ G¹³ 1066 R⁶ G¹⁴ 1067 R⁶ G¹⁵ 1068 R⁶ G¹⁶ 1069 R⁷ G¹³ 1070 R⁷ G¹⁴ 1071 R⁷ G¹⁵ 1072 R⁷ G¹⁶ 1073 R⁸ G¹³ 1074 R⁸ G¹⁴ 1075 R⁸ G¹⁵ 1076 R⁸ G¹⁶ 1077 R⁹ G¹³ 1078 R⁹ G¹⁴ 1079 R⁹ G¹⁵ 1080 R⁹ G¹⁶ 1081 R¹⁰ G¹³ 1082 R¹⁰ G¹⁴ 1083 R¹⁰ G¹⁵ 1084 R¹⁰ G¹⁶ 1085 R¹¹ G¹³ 1086 R¹¹ G¹⁴ 1087 R¹¹ G¹⁵ 1088 R¹¹ G¹⁶ 1089 R¹² G¹³ 1090 R¹² G¹⁴ 1091 R¹² G¹⁵ 1092 R¹² G¹⁶ 1093 R¹³ G¹³ 1094 R¹³ G¹⁴ 1095 R¹³ G¹⁵ 1096 R¹³ G¹⁶ 1097 R¹⁴ G¹³ 1098 R¹⁴ G¹⁴ 1099 R¹⁴ G¹⁵ 1100 R¹⁴ G¹⁶ 1101 R¹⁵ G¹³ 1102 R¹⁵ G¹⁴ 1103 R¹⁵ G¹⁵ 1104 R¹⁵ G¹⁶ 1105 R¹⁶ G¹³ 1106 R¹⁶ G¹⁴ 1107 R¹⁶ G¹⁵ 1108 R¹⁶ G¹⁶ 1109 R¹⁷ G¹³ 1110 R¹⁷ G¹⁴ 1111 R¹⁷ G¹⁵ 1112 R¹⁷ G¹⁶ 1113 R¹⁸ G¹³ 1114 R¹⁸ G¹⁴ 1115 R¹⁸ G¹⁵ 1116 R¹⁸ G¹⁶ 1117 R¹⁹ G¹³ 1118 R¹⁹ G¹⁴ 1119 R¹⁹ G¹⁵ 1120 R¹⁹ G¹⁶ 1121 R²⁰ G¹³ 1122 R²⁰ G¹⁴ 1123 R²⁰ G¹⁵ 1124 R²⁰ G¹⁶ 1125 R²¹ G¹³ 1126 R²¹ G¹⁴ 1127 R²¹ G¹⁵ 1128 R²¹ G¹⁶ 1129 R²² G¹³ 1130 R²² G¹⁴ 1131 R²² G¹⁵ 1132 R²² G¹⁶ 1133 R²³ G¹³ 1134 R²³ G¹⁴ 1135 R²³ G¹⁵ 1136 R²³ G¹⁶ 1137 R²⁴ G¹³ 1138 R²⁴ G¹⁴ 1139 R²⁴ G¹⁵ 1140 R²⁴ G¹⁶ 1141 R²⁵ G¹³ 1142 R²⁵ G¹⁴ 1143 R²⁵ G¹⁵ 1144 R²⁵ G¹⁶ 1145 R²⁶ G¹³ 1146 R²⁶ G¹⁴ 1147 R²⁶ G¹⁵ 1148 R²⁶ G¹⁶ 1149 R²⁷ G¹³ 1150 R²⁷ G¹⁴ 1151 R²⁷ G¹⁵ 1152 R²⁷ G¹⁶ 1153 R²⁸ G¹³ 1154 R²⁸ G¹⁴ 1155 R²⁸ G¹⁵ 1156 R²⁸ G¹⁶ 1157 R²⁹ G¹³ 1158 R²⁹ G¹⁴ 1159 R²⁹ G¹⁵ 1160 R²⁹ G¹⁶ 1161 R³⁰ G¹³ 1162 R³⁰ G¹⁴ 1163 R³⁰ G¹⁵ 1164 R³⁰ G¹⁶ 1165 R³¹ G¹³ 1166 R³¹ G¹⁴ 1167 R³¹ G¹⁵ 1168 R³¹ G¹⁶ 1169 R³² G¹³ 1170 R³² G¹⁴ 1171 R³² G¹⁵ 1172 R³² G¹⁶ 1173 R³³ G¹³ 1174 R³³ G¹⁴ 1175 R³³ G¹⁵ 1176 R³³ G¹⁶ 1177 R³⁴ G¹³ 1178 R³⁴ G¹⁴ 1179 R³⁴ G¹⁵ 1180 R³⁴ G¹⁶ 1181 R³⁵ G¹³ 1182 R³⁵ G¹⁴ 1183 R³⁵ G¹⁵ 1184 R³⁵ G¹⁶ 1185 R³⁶ G¹³ 1186 R³⁶ G¹⁴ 1187 R³⁶ G¹⁵ 1188 R³⁶ G¹⁶ 1189 R³⁷ G¹³ 1190 R³⁷ G¹⁴ 1191 R³⁷ G¹⁵ 1192 R³⁷ G¹⁶ 1193 R³⁸ G¹³ 1194 R³⁸ G¹⁴ 1195 R³⁸ G¹⁵ 1196 R³⁸ G¹⁶ 1197 R³⁹ G¹³ 1198 R³⁹ G¹⁴ 1199 R³⁹ G¹⁵ 1200 R³⁹ G¹⁶ 1201 R⁴⁰ G¹³ 1202 R⁴⁰ G¹⁴ 1203 R⁴⁰ G¹⁵ 1204 R⁴⁰ G¹⁶ 1205 R⁴¹ G¹³ 1206 R⁴¹ G¹⁴ 1207 R⁴¹ G¹⁵ 1208 R⁴¹ G¹⁶ 1209 R⁴² G¹³ 1210 R⁴² G¹⁴ 1211 R⁴² G¹⁵ 1212 R⁴² G¹⁶ 1213 R⁴³ G¹³ 1214 R⁴³ G¹⁴ 1215 R⁴³ G¹⁵ 1216 R⁴³ G¹⁶ 1217 R⁴⁴ G¹³ 1218 R⁴⁴ G¹⁴ 1219 R⁴⁴ G¹⁵ 1220 R⁴⁴ G¹⁶ 1221 R⁴⁵ G¹³ 1222 R⁴⁵ G¹⁴ 1223 R⁴⁵ G¹⁵ 1224 R⁴⁵ G¹⁶ 1225 R⁴⁶ G¹³ 1226 R⁴⁶ G¹⁴ 1227 R⁴⁶ G¹⁵ 1228 R⁴⁶ G¹⁶ 1229 R⁴⁷ G¹³ 1230 R⁴⁷ G¹⁴ 1231 R⁴⁷ G¹⁵ 1232 R⁴⁷ G¹⁶ 1233 R⁴⁸ G¹³ 1234 R⁴⁸ G¹⁴ 1235 R⁴⁸ G¹⁵ 1236 R⁴⁸ G¹⁶ 1237 R⁴⁹ G¹³ 1238 R⁴⁹ G¹⁴ 1239 R⁴⁹ G¹⁵ 1240 R⁴⁹ G¹⁶ 1241 R⁵⁰ G¹³ 1242 R⁵⁰ G¹⁴ 1243 R⁵⁰ G¹⁵ 1244 R⁵⁰ G¹⁶ 1245 R⁵¹ G¹³ 1246 R⁵¹ G¹⁴ 1247 R⁵¹ G¹⁵ 1248 R⁵¹ G¹⁶ 1249 R⁵² G¹³ 1250 R⁵² G¹⁴ 1251 R⁵² G¹⁵ 1252 R⁵² G¹⁶ 1253 R⁵³ G¹³ 1254 R⁵³ G¹⁴ 1255 R⁵³ G¹⁵ 1256 R⁵³ G¹⁶ 1257 R⁵⁴ G¹³ 1258 R⁵⁴ G¹⁴ 1259 R⁵⁴ G¹⁵ 1260 R⁵⁴ G¹⁶ 1261 R⁵⁵ G¹³ 1262 R⁵⁵ G¹⁴ 1263 R⁵⁵ G¹⁵ 1264 R⁵⁵ G¹⁶ 1265 R⁵⁶ G¹³ 1266 R⁵⁶ G¹⁴ 1267 R⁵⁶ G¹⁵ 1268 R⁵⁶ G¹⁶ 1269 R⁵⁷ G¹³ 1270 R⁵⁷ G¹⁴ 1271 R⁵⁷ G¹⁵ 1272 R⁵⁷ G¹⁶ 1273 R⁵⁸ G¹³ 1274 R⁵⁸ G¹⁴ 1275 R⁵⁸ G¹⁵ 1276 R⁵⁸ G¹⁶ 1277 R⁵⁹ G¹³ 1278 R⁵⁹ G¹⁴ 1279 R⁵⁹ G¹⁵ 1280 R⁵⁹ G¹⁶ 1281 R⁶⁰ G¹³ 1282 R⁶⁰ G¹⁴ 1283 R⁶⁰ G¹⁵ 1284 R⁶⁰ G¹⁶ 1285 R⁶¹ G¹³ 1286 R⁶¹ G¹⁴ 1287 R⁶¹ G¹⁵ 1288 R⁶¹ G¹⁶ 1289 R⁶² G¹³ 1290 R⁶² G¹⁴ 1291 R⁶² G¹⁵ 1292 R⁶² G¹⁶ 1293 R⁶³ G¹³ 1294 R⁶³ G¹⁴ 1295 R⁶³ G¹⁵ 1296 R⁶³ G¹⁶ 1297 R⁶⁴ G¹³ 1298 R⁶⁴ G¹⁴ 1299 R⁶⁴ G¹⁵ 1300 R⁶⁴ G¹⁶ 1301 R⁶⁵ G¹³ 1302 R⁶⁵ G¹⁴ 1303 R⁶⁵ G¹⁵ 1304 R⁶⁵ G¹⁶ 1305 R⁶⁶ G¹³ 1306 R⁶⁶ G¹⁴ 1307 R⁶⁶ G¹⁵ 1308 R⁶⁶ G¹⁶ 1309 R⁶⁷ G¹³ 1310 R⁶⁷ G¹⁴ 1311 R⁶⁷ G¹⁵ 1312 R⁶⁷ G¹⁶ 1313 R⁶⁸ G¹³ 1314 R⁶⁸ G¹⁴ 1315 R⁶⁸ G¹⁵ 1316 R⁶⁸ G¹⁶ 1317 R⁶⁹ G¹³ 1318 R⁶⁹ G¹⁴ 1319 R⁶⁹ G¹⁵ 1320 R⁶⁹ G¹⁶ 1321 R⁷⁰ G¹³ 1322 R⁷⁰ G¹⁴ 1323 R⁷⁰ G¹⁵ 1324 R⁷⁰ G¹⁶ 1325 R⁷¹ G¹³ 1326 R⁷¹ G¹⁴ 1327 R⁷¹ G¹⁵ 1328 R⁷¹ G¹⁶ 1329 R⁷² G¹³ 1330 R⁷² G¹⁴ 1331 R⁷² G¹⁵ 1332 R⁷² G¹⁶ 1333 R⁷³ G¹³ 1334 R⁷³ G¹⁴ 1335 R⁷³ G¹⁵ 1336 R⁷³ G¹⁶ 1337 R⁷⁴ G¹³ 1338 R⁷⁴ G¹⁴ 1339 R⁷⁴ G¹⁵ 1340 R⁷⁴ G¹⁶ 1341 R⁷⁵ G¹³ 1342 R⁷⁵ G¹⁴ 1343 R⁷⁵ G¹⁵ 1344 R⁷⁵ G¹⁶ 1345 R⁷⁶ G¹³ 1346 R⁷⁶ G¹⁴ 1347 R⁷⁶ G¹⁵ 1348 R⁷⁶ G¹⁶ 1349 R⁷⁷ G¹³ 1350 R⁷⁷ G¹⁴ 1351 R⁷⁷ G¹⁵ 1352 R⁷⁷ G¹⁶ 1353 R⁷⁸ G¹³ 1354 R⁷⁸ G¹⁴ 1355 R⁷⁸ G¹⁵ 1356 R⁷⁸ G¹⁶ 1357 R⁷⁹ G¹³ 1358 R⁷⁹ G¹⁴ 1359 R⁷⁹ G¹⁵ 1360 R⁷⁹ G¹⁶ 1361 R⁸⁰ G¹³ 1362 R⁸⁰ G¹⁴ 1363 R⁸⁰ G¹⁵ 1364 R⁸⁰ G¹⁶ 1365 R⁸¹ G¹³ 1366 R⁸¹ G¹⁴ 1367 R⁸¹ G¹⁵ 1368 R⁸¹ G¹⁶ 1369 R⁸² G¹³ 1370 R⁸² G¹⁴ 1371 R⁸² G¹⁵ 1372 R⁸² G¹⁶ 1373 R⁸³ G¹³ 1374 R⁸³ G¹⁴ 1375 R⁸³ G¹⁵ 1376 R⁸³ G¹⁶ 1377 R⁸⁴ G¹³ 1378 R⁸⁴ G¹⁴ 1379 R⁸⁴ G¹⁵ 1380 R⁸⁴ G¹⁶ 1381 R⁸⁵ G¹³ 1382 R⁸⁵ G¹⁴ 1383 R⁸⁵ G¹⁵ 1384 R⁸⁵ G¹⁶ 1385 R⁸⁶ G¹³ 1386 R⁸⁶ G¹⁴ 1387 R⁸⁶ G¹⁵ 1388 R⁸⁶ G¹⁶ 1389 R⁸⁷ G¹³ 1390 R⁸⁷ G¹⁴ 1391 R⁸⁷ G¹⁵ 1392 R⁸⁷ G¹⁶ 1393 R¹ G¹⁷ 1394 R¹ G¹⁸ 1395 R¹ G¹⁹ 1396 R¹ G²⁰ 1397 R² G¹⁷ 1398 R² G¹⁸ 1399 R² G¹⁹ 1400 R² G²⁰ 1401 R³ G¹⁷ 1402 R³ G¹⁸ 1403 R³ G¹⁹ 1404 R³ G²⁰ 1405 R⁴ G¹⁷ 1406 R⁴ G¹⁸ 1407 R⁴ G¹⁹ 1408 R⁴ G²⁰ 1409 R⁵ G¹⁷ 1410 R⁵ G¹⁸ 1411 R⁵ G¹⁹ 1412 R⁵ G²⁰ 1413 R⁶ G¹⁷ 1414 R⁶ G¹⁸ 1415 R⁶ G¹⁹ 1416 R⁶ G²⁰ 1417 R⁷ G¹⁷ 1418 R⁷ G¹⁸ 1419 R⁷ G¹⁹ 1420 R⁷ G²⁰ 1421 R⁸ G¹⁷ 1422 R⁸ G¹⁸ 1423 R⁸ G¹⁹ 1424 R⁸ G²⁰ 1425 R⁹ G¹⁷ 1426 R⁹ G¹⁸ 1427 R⁹ G¹⁹ 1428 R⁹ G²⁰ 1429 R¹⁰ G¹⁷ 1430 R¹⁰ G¹⁸ 1431 R¹⁰ G¹⁹ 1432 R¹⁰ G²⁰ 1433 R¹¹ G¹⁷ 1434 R¹¹ G¹⁸ 1435 R¹¹ G¹⁹ 1436 R¹¹ G²⁰ 1437 R¹² G¹⁷ 1438 R¹² G¹⁸ 1439 R¹² G¹⁹ 1440 R¹² G²⁰ 1441 R¹³ G¹⁷ 1442 R¹³ G¹⁸ 1443 R¹³ G¹⁹ 1444 R¹³ G²⁰ 1445 R¹⁴ G¹⁷ 1446 R¹⁴ G¹⁸ 1447 R¹⁴ G¹⁹ 1448 R¹⁴ G²⁰ 1449 R¹⁵ G¹⁷ 1450 R¹⁵ G¹⁸ 1451 R¹⁵ G¹⁹ 1452 R¹⁵ G²⁰ 1453 R¹⁶ G¹⁷ 1454 R¹⁶ G¹⁸ 1455 R¹⁶ G¹⁹ 1456 R¹⁶ G²⁰ 1457 R¹⁷ G¹⁷ 1458 R¹⁷ G¹⁸ 1459 R¹⁷ G¹⁹ 1460 R¹⁷ G²⁰ 1461 R¹⁸ G¹⁷ 1462 R¹⁸ G¹⁸ 1463 R¹⁸ G¹⁹ 1464 R¹⁸ G²⁰ 1465 R¹⁹ G¹⁷ 1466 R¹⁹ G¹⁸ 1467 R¹⁹ G¹⁹ 1468 R¹⁹ G²⁰ 1469 R²⁰ G¹⁷ 1470 R²⁰ G¹⁸ 1471 R²⁰ G¹⁹ 1472 R²⁰ G²⁰ 1473 R²¹ G¹⁷ 1474 R²¹ G¹⁸ 1475 R²¹ G¹⁹ 1476 R²¹ G²⁰ 1477 R²² G¹⁷ 1478 R²² G¹⁸ 1479 R²² G¹⁹ 1480 R²² G²⁰ 1481 R²³ G¹⁷ 1482 R²³ G¹⁸ 1483 R²³ G¹⁹ 1484 R²³ G²⁰ 1485 R²⁴ G¹⁷ 1486 R²⁴ G¹⁸ 1487 R²⁴ G¹⁹ 1488 R²⁴ G²⁰ 1489 R²⁵ G¹⁷ 1490 R²⁵ G¹⁸ 1491 R²⁵ G¹⁹ 1492 R²⁵ G²⁰ 1493 R²⁶ G¹⁷ 1494 R²⁶ G¹⁸ 1495 R²⁶ G¹⁹ 1496 R²⁶ G²⁰ 1497 R²⁷ G¹⁷ 1498 R²⁷ G¹⁸ 1499 R²⁷ G¹⁹ 1500 R²⁷ G²⁰ 1501 R²⁸ G¹⁷ 1502 R²⁸ G¹⁸ 1503 R²⁸ G¹⁹ 1504 R²⁸ G²⁰ 1505 R²⁹ G¹⁷ 1506 R²⁹ G¹⁸ 1507 R²⁹ G¹⁹ 1508 R²⁹ G²⁰ 1509 R³⁰ G¹⁷ 1510 R³⁰ G¹⁸ 1511 R³⁰ G¹⁹ 1512 R³⁰ G²⁰ 1513 R³¹ G¹⁷ 1514 R³¹ G¹⁸ 1515 R³¹ G¹⁹ 1516 R³¹ G²⁰ 1517 R³² G¹⁷ 1518 R³² G¹⁸ 1519 R³² G¹⁹ 1520 R³² G²⁰ 1521 R³³ G¹⁷ 1522 R³³ G¹⁸ 1523 R³³ G¹⁹ 1524 R³³ G²⁰ 1525 R³⁴ G¹⁷ 1526 R³⁴ G¹⁸ 1527 R³⁴ G¹⁹ 1528 R³⁴ G²⁰ 1529 R³⁵ G¹⁷ 1530 R³⁵ G¹⁸ 1531 R³⁵ G¹⁹ 1532 R³⁵ G²⁰ 1533 R³⁶ G¹⁷ 1534 R³⁶ G¹⁸ 1535 R³⁶ G¹⁹ 1536 R³⁶ G²⁰ 1537 R³⁷ G¹⁷ 1538 R³⁷ G¹⁸ 1539 R³⁷ G¹⁹ 1540 R³⁷ G²⁰ 1541 R³⁸ G¹⁷ 1542 R³⁸ G¹⁸ 1543 R³⁸ G¹⁹ 1544 R³⁸ G²⁰ 1545 R³⁹ G¹⁷ 1546 R³⁹ G¹⁸ 1547 R³⁹ G¹⁹ 1548 R³⁹ G²⁰ 1549 R⁴⁰ G¹⁷ 1550 R⁴⁰ G¹⁸ 1551 R⁴⁰ G¹⁹ 1552 R⁴⁰ G²⁰ 1553 R⁴¹ G¹⁷ 1554 R⁴¹ G¹⁸ 1555 R⁴¹ G¹⁹ 1556 R⁴¹ G²⁰ 1557 R⁴² G¹⁷ 1558 R⁴² G¹⁸ 1559 R⁴² G¹⁹ 1560 R⁴² G²⁰ 1561 R⁴³ G¹⁷ 1562 R⁴³ G¹⁸ 1563 R⁴³ G¹⁹ 1564 R⁴³ G²⁰ 1565 R⁴⁴ G¹⁷ 1566 R⁴⁴ G¹⁸ 1567 R⁴⁴ G¹⁹ 1568 R⁴⁴ G²⁰ 1569 R⁴⁵ G¹⁷ 1570 R⁴⁵ G¹⁸ 1571 R⁴⁵ G¹⁹ 1572 R⁴⁵ G²⁰ 1573 R⁴⁶ G¹⁷ 1574 R⁴⁶ G¹⁸ 1575 R⁴⁶ G¹⁹ 1576 R⁴⁶ G²⁰ 1577 R⁴⁷ G¹⁷ 1578 R⁴⁷ G¹⁸ 1579 R⁴⁷ G¹⁹ 1580 R⁴⁷ G²⁰ 1581 R⁴⁸ G¹⁷ 1582 R⁴⁸ G¹⁸ 1583 R⁴⁸ G¹⁹ 1584 R⁴⁸ G²⁰ 1585 R⁴⁹ G¹⁷ 1586 R⁴⁹ G¹⁸ 1587 R⁴⁹ G¹⁹ 1588 R⁴⁹ G²⁰ 1589 R⁵⁰ G¹⁷ 1590 R⁵⁰ G¹⁸ 1591 R⁵⁰ G¹⁹ 1592 R⁵⁰ G²⁰ 1593 R⁵¹ G¹⁷ 1594 R⁵¹ G¹⁸ 1595 R⁵¹ G¹⁹ 1596 R⁵¹ G²⁰ 1597 R⁵² G¹⁷ 1598 R⁵² G¹⁸ 1599 R⁵² G¹⁹ 1600 R⁵² G²⁰ 1601 R⁵³ G¹⁷ 1602 R⁵³ G¹⁸ 1603 R⁵³ G¹⁹ 1604 R⁵³ G²⁰ 1605 R⁵⁴ G¹⁷ 1606 R⁵⁴ G¹⁸ 1607 R⁵⁴ G¹⁹ 1608 R⁵⁴ G²⁰ 1609 R⁵⁵ G¹⁷ 1610 R⁵⁵ G¹⁸ 1611 R⁵⁵ G¹⁹ 1612 R⁵⁵ G²⁰ 1613 R⁵⁶ G¹⁷ 1614 R⁵⁶ G¹⁸ 1615 R⁵⁶ G¹⁹ 1616 R⁵⁶ G²⁰ 1617 R⁵⁷ G¹⁷ 1618 R⁵⁷ G¹⁸ 1619 R⁵⁷ G¹⁹ 1620 R⁵⁷ G²⁰ 1621 R⁵⁸ G¹⁷ 1622 R⁵⁸ G¹⁸ 1623 R⁵⁸ G¹⁹ 1624 R⁵⁸ G²⁰ 1625 R⁵⁹ G¹⁷ 1626 R⁵⁹ G¹⁸ 1627 R⁵⁹ G¹⁹ 1628 R⁵⁹ G²⁰ 1629 R⁶⁰ G¹⁷ 1630 R⁶⁰ G¹⁸ 1631 R⁶⁰ G¹⁹ 1632 R⁶⁰ G²⁰ 1633 R⁶¹ G¹⁷ 1634 R⁶¹ G¹⁸ 1635 R⁶¹ G¹⁹ 1636 R⁶¹ G²⁰ 1637 R⁶² G¹⁷ 1638 R⁶² G¹⁸ 1639 R⁶² G¹⁹ 1640 R⁶² G²⁰ 1641 R⁶³ G¹⁷ 1642 R⁶³ G¹⁸ 1643 R⁶³ G¹⁹ 1644 R⁶³ G²⁰ 1645 R⁶⁴ G¹⁷ 1646 R⁶⁴ G¹⁸ 1647 R⁶⁴ G¹⁹ 1648 R⁶⁴ G²⁰ 1649 R⁶⁵ G¹⁷ 1650 R⁶⁵ G¹⁸ 1651 R⁶⁵ G¹⁹ 1652 R⁶⁵ G²⁰ 1653 R⁶⁶ G¹⁷ 1654 R⁶⁶ G¹⁸ 1655 R⁶⁶ G¹⁹ 1656 R⁶⁶ G²⁰ 1657 R⁶⁷ G¹⁷ 1658 R⁶⁷ G¹⁸ 1659 R⁶⁷ G¹⁹ 1660 R⁶⁷ G²⁰ 1661 R⁶⁸ G¹⁷ 1662 R⁶⁸ G¹⁸ 1663 R⁶⁸ G¹⁹ 1664 R⁶⁸ G²⁰ 1665 R⁶⁹ G¹⁷ 1666 R⁶⁹ G¹⁸ 1667 R⁶⁹ G¹⁹ 1668 R⁶⁹ G²⁰ 1669 R⁷⁰ G¹⁷ 1670 R⁷⁰ G¹⁸ 1671 R⁷⁰ G¹⁹ 1672 R⁷⁰ G²⁰ 1673 R⁷¹ G¹⁷ 1674 R⁷¹ G¹⁸ 1675 R⁷¹ G¹⁹ 1676 R⁷¹ G²⁰ 1677 R⁷² G¹⁷ 1678 R⁷² G¹⁸ 1679 R⁷² G¹⁹ 1680 R⁷² G²⁰ 1681 R⁷³ G¹⁷ 1682 R⁷³ G¹⁸ 1683 R⁷³ G¹⁹ 1684 R⁷³ G²⁰ 1685 R⁷⁴ G¹⁷ 1686 R⁷⁴ G¹⁸ 1687 R⁷⁴ G¹⁹ 1688 R⁷⁴ G²⁰ 1689 R⁷⁵ G¹⁷ 1690 R⁷⁵ G¹⁸ 1691 R⁷⁵ G¹⁹ 1692 R⁷⁵ G²⁰ 1693 R⁷⁶ G¹⁷ 1694 R⁷⁶ G¹⁸ 1695 R⁷⁶ G¹⁹ 1696 R⁷⁶ G²⁰ 1697 R⁷⁷ G¹⁷ 1698 R⁷⁷ G¹⁸ 1699 R⁷⁷ G¹⁹ 1700 R⁷⁷ G²⁰ 1701 R⁷⁸ G¹⁷ 1702 R⁷⁸ G¹⁸ 1703 R⁷⁸ G¹⁹ 1704 R⁷⁸ G²⁰ 1705 R⁷⁹ G¹⁷ 1706 R⁷⁹ G¹⁸ 1707 R⁷⁹ G¹⁹ 1708 R⁷⁹ G²⁰ 1709 R⁸⁰ G¹⁷ 1710 R⁸⁰ G¹⁸ 1711 R⁸⁰ G¹⁹ 1712 R⁸⁰ G²⁰ 1713 R⁸¹ G¹⁷ 1714 R⁸¹ G¹⁸ 1715 R⁸¹ G¹⁹ 1716 R⁸¹ G²⁰ 1717 R⁸² G¹⁷ 1718 R⁸² G¹⁸ 1719 R⁸² G¹⁹ 1720 R⁸² G²⁰ 1721 R⁸³ G¹⁷ 1722 R⁸³ G¹⁸ 1723 R⁸³ G¹⁹ 1724 R⁸³ G²⁰ 1725 R⁸⁴ G¹⁷ 1726 R⁸⁴ G¹⁸ 1727 R⁸⁴ G¹⁹ 1728 R⁸⁴ G²⁰ 1729 R⁸⁵ G¹⁷ 1730 R⁸⁵ G¹⁸ 1731 R⁸⁵ G¹⁹ 1732 R⁸⁵ G²⁰ 1733 R⁸⁶ G¹⁷ 1734 R⁸⁶ G¹⁸ 1735 R⁸⁶ G¹⁹ 1736 R⁸⁶ G²⁰ 1737 R⁸⁷ G¹⁷ 1738 R⁸⁷ G¹⁸ 1739 R⁸⁷ G¹⁹ 1740 R⁸⁷ G²⁰ 1741 R¹ G²¹ 1742 R¹ G²² 1743 R¹ G²³ 1744 R¹ G²⁴ 1745 R² G²¹ 1746 R² G²² 1747 R² G²³ 1748 R² G²⁴ 1749 R³ G²¹ 1750 R³ G²² 1751 R³ G²³ 1752 R³ G²⁴ 1753 R⁴ G²¹ 1754 R⁴ G²² 1755 R⁴ G²³ 1756 R⁴ G²⁴ 1757 R⁵ G²¹ 1758 R⁵ G²² 1759 R⁵ G²³ 1760 R⁵ G²⁴ 1761 R⁶ G²¹ 1762 R⁶ G²² 1763 R⁶ G²³ 1764 R⁶ G²⁴ 1765 R⁷ G²¹ 1766 R⁷ G²² 1767 R⁷ G²³ 1768 R⁷ G²⁴ 1769 R⁸ G²¹ 1770 R⁸ G²² 1771 R⁸ G²³ 1772 R⁸ G²⁴ 1773 R⁹ G²¹ 1774 R⁹ G²² 1775 R⁹ G²³ 1776 R⁹ G²⁴ 1777 R¹⁰ G²¹ 1778 R¹⁰ G²² 1779 R¹⁰ G²³ 1780 R¹⁰ G²⁴ 1781 R¹¹ G²¹ 1782 R¹¹ G²² 1783 R¹¹ G²³ 1784 R¹¹ G²⁴ 1785 R¹² G²¹ 1786 R¹² G²² 1787 R¹² G²³ 1788 R¹² G²⁴ 1789 R¹³ G²¹ 1790 R¹³ G²² 1791 R¹³ G²³ 1792 R¹³ G²⁴ 1793 R¹⁴ G²¹ 1794 R¹⁴ G²² 1795 R¹⁴ G²³ 1796 R¹⁴ G²⁴ 1797 R¹⁵ G²¹ 1798 R¹⁵ G²² 1799 R¹⁵ G²³ 1800 R¹⁵ G²⁴ 1801 R¹⁶ G²¹ 1802 R¹⁶ G²² 1803 R¹⁶ G²³ 1804 R¹⁶ G²⁴ 1805 R¹⁷ G²¹ 1806 R¹⁷ G²² 1807 R¹⁷ G²³ 1808 R¹⁷ G²⁴ 1809 R¹⁸ G²¹ 1810 R¹⁸ G²² 1811 R¹⁸ G²³ 1812 R¹⁸ G²⁴ 1813 R¹⁹ G²¹ 1814 R¹⁹ G²² 1815 R¹⁹ G²³ 1816 R¹⁹ G²⁴ 1817 R²⁰ G²¹ 1818 R²⁰ G²² 1819 R²⁰ G²³ 1820 R²⁰ G²⁴ 1821 R²¹ G²¹ 1822 R²¹ G²² 1823 R²¹ G²³ 1824 R²¹ G²⁴ 1825 R²² G²¹ 1826 R²² G²² 1827 R²² G²³ 1828 R²² G²⁴ 1829 R²³ G²¹ 1830 R²³ G²² 1831 R²³ G²³ 1832 R²³ G²⁴ 1833 R²⁴ G²¹ 1834 R²⁴ G²² 1835 R²⁴ G²³ 1836 R²⁴ G²⁴ 1837 R²⁵ G²¹ 1838 R²⁵ G²² 1839 R²⁵ G²³ 1840 R²⁵ G²⁴ 1841 R²⁶ G²¹ 1842 R²⁶ G²² 1843 R²⁶ G²³ 1844 R²⁶ G²⁴ 1845 R²⁷ G²¹ 1846 R²⁷ G²² 1847 R²⁷ G²³ 1848 R²⁷ G²⁴ 1849 R²⁸ G²¹ 1850 R²⁸ G²² 1851 R²⁸ G²³ 1852 R²⁸ G²⁴ 1853 R²⁹ G²¹ 1854 R²⁹ G²² 1855 R²⁹ G²³ 1856 R²⁹ G²⁴ 1857 R³⁰ G²¹ 1858 R³⁰ G²² 1859 R³⁰ G²³ 1860 R³⁰ G²⁴ 1861 R³¹ G²¹ 1862 R³¹ G²² 1863 R³¹ G²³ 1864 R³¹ G²⁴ 1865 R³² G²¹ 1866 R³² G²² 1867 R³² G²³ 1868 R³² G²⁴ 1869 R³³ G²¹ 1870 R³³ G²² 1871 R³³ G²³ 1872 R³³ G²⁴ 1873 R³⁴ G²¹ 1874 R³⁴ G²² 1875 R³⁴ G²³ 1876 R³⁴ G²⁴ 1877 R³⁵ G²¹ 1878 R³⁵ G²² 1879 R³⁵ G²³ 1880 R³⁵ G²⁴ 1881 R³⁶ G²¹ 1882 R³⁶ G²² 1883 R³⁶ G²³ 1884 R³⁶ G²⁴ 1885 R³⁷ G²¹ 1886 R³⁷ G²² 1887 R³⁷ G²³ 1888 R³⁷ G²⁴ 1889 R³⁸ G²¹ 1890 R³⁸ G²² 1891 R³⁸ G²³ 1892 R³⁸ G²⁴ 1893 R³⁹ G²¹ 1894 R³⁹ G²² 1895 R³⁹ G²³ 1896 R³⁹ G²⁴ 1897 R⁴⁰ G²¹ 1898 R⁴⁰ G²² 1899 R⁴⁰ G²³ 1900 R⁴⁰ G²⁴ 1901 R⁴¹ G²¹ 1902 R⁴¹ G²² 1903 R⁴¹ G²³ 1904 R⁴¹ G²⁴ 1905 R⁴² G²¹ 1906 R⁴² G²² 1907 R⁴² G²³ 1908 R⁴² G²⁴ 1909 R⁴³ G²¹ 1910 R⁴³ G²² 1911 R⁴³ G²³ 1912 R⁴³ G²⁴ 1913 R⁴⁴ G²¹ 1914 R⁴⁴ G²² 1915 R⁴⁴ G²³ 1916 R⁴⁴ G²⁴ 1917 R⁴⁵ G²¹ 1918 R⁴⁵ G²² 1919 R⁴⁵ G²³ 1920 R⁴⁵ G²⁴ 1921 R⁴⁶ G²¹ 1922 R⁴⁶ G²² 1923 R⁴⁶ G²³ 1924 R⁴⁶ G²⁴ 1925 R⁴⁷ G²¹ 1926 R⁴⁷ G²² 1927 R⁴⁷ G²³ 1928 R⁴⁷ G²⁴ 1929 R⁴⁸ G²¹ 1930 R⁴⁸ G²² 1931 R⁴⁸ G²³ 1932 R⁴⁸ G²⁴ 1933 R⁴⁹ G²¹ 1934 R⁴⁹ G²² 1935 R⁴⁹ G²³ 1936 R⁴⁹ G²⁴ 1937 R⁵⁰ G²¹ 1938 R⁵⁰ G²² 1939 R⁵⁰ G²³ 1940 R⁵⁰ G²⁴ 1941 R⁵¹ G²¹ 1942 R⁵¹ G²² 1943 R⁵¹ G²³ 1944 R⁵¹ G²⁴ 1945 R⁵² G²¹ 1946 R⁵² G²² 1947 R⁵² G²³ 1948 R⁵² G²⁴ 1949 R⁵³ G²¹ 1950 R⁵³ G²² 1951 R⁵³ G²³ 1952 R⁵³ G²⁴ 1953 R⁵⁴ G²¹ 1954 R⁵⁴ G²² 1955 R⁵⁴ G²³ 1956 R⁵⁴ G²⁴ 1957 R⁵⁵ G²¹ 1958 R⁵⁵ G²² 1959 R⁵⁵ G²³ 1960 R⁵⁵ G²⁴ 1961 R⁵⁶ G²¹ 1962 R⁵⁶ G²² 1963 R⁵⁶ G²³ 1964 R⁵⁶ G²⁴ 1965 R⁵⁷ G²¹ 1966 R⁵⁷ G²² 1967 R⁵⁷ G²³ 1968 R⁵⁷ G²⁴ 1969 R⁵⁸ G²¹ 1970 R⁵⁸ G²² 1971 R⁵⁸ G²³ 1972 R⁵⁸ G²⁴ 1973 R⁵⁹ G²¹ 1974 R⁵⁹ G²² 1975 R⁵⁹ G²³ 1976 R⁵⁹ G²⁴ 1977 R⁶⁰ G²¹ 1978 R⁶⁰ G²² 1979 R⁶⁰ G²³ 1980 R⁶⁰ G²⁴ 1981 R⁶¹ G²¹ 1982 R⁶¹ G²² 1983 R⁶¹ G²³ 1984 R⁶¹ G²⁴ 1985 R⁶² G²¹ 1986 R⁶² G²² 1987 R⁶² G²³ 1988 R⁶² G²⁴ 1989 R⁶³ G²¹ 1990 R⁶³ G²² 1991 R⁶³ G²³ 1992 R⁶³ G²⁴ 1993 R⁶⁴ G²¹ 1994 R⁶⁴ G²² 1995 R⁶⁴ G²³ 1996 R⁶⁴ G²⁴ 1997 R⁶⁵ G²¹ 1998 R⁶⁵ G²² 1999 R⁶⁵ G²³ 2000 R⁶⁵ G²⁴ 2001 R⁶⁶ G²¹ 2002 R⁶⁶ G²² 2003 R⁶⁶ G²³ 2004 R⁶⁶ G²⁴ 2005 R⁶⁷ G²¹ 2006 R⁶⁷ G²² 2007 R⁶⁷ G²³ 2008 R⁶⁷ G²⁴ 2009 R⁶⁸ G²¹ 2010 R⁶⁸ G²² 2011 R⁶⁸ G²³ 2012 R⁶⁸ G²⁴ 2013 R⁶⁹ G²¹ 2014 R⁶⁹ G²² 2015 R⁶⁹ G²³ 2016 R⁶⁹ G²⁴ 2017 R⁷⁰ G²¹ 2018 R⁷⁰ G²² 2019 R⁷⁰ G²³ 2020 R⁷⁰ G²⁴ 2021 R⁷¹ G²¹ 2022 R⁷¹ G²² 2023 R⁷¹ G²³ 2024 R⁷¹ G²⁴ 2025 R⁷² G²¹ 2026 R⁷² G²² 2027 R⁷² G²³ 2028 R⁷² G²⁴ 2029 R⁷³ G²¹ 2030 R⁷³ G²² 2031 R⁷³ G²³ 2032 R⁷³ G²⁴ 2033 R⁷⁴ G²¹ 2034 R⁷⁴ G²² 2035 R⁷⁴ G²³ 2036 R⁷⁴ G²⁴ 2037 R⁷⁵ G²¹ 2038 R⁷⁵ G²² 2039 R⁷⁵ G²³ 2040 R⁷⁵ G²⁴ 2041 R⁷⁶ G²¹ 2042 R⁷⁶ G²² 2043 R⁷⁶ G²³ 2044 R⁷⁶ G²⁴ 2045 R⁷⁷ G²¹ 2046 R⁷⁷ G²² 2047 R⁷⁷ G²³ 2048 R⁷⁷ G²⁴ 2049 R⁷⁸ G²¹ 2050 R⁷⁸ G²² 2051 R⁷⁸ G²³ 2052 R⁷⁸ G²⁴ 2053 R⁷⁹ G²¹ 2054 R⁷⁹ G²² 2055 R⁷⁹ G²³ 2056 R⁷⁹ G²⁴ 2057 R⁸⁰ G²¹ 2058 R⁸⁰ G²² 2059 R⁸⁰ G²³ 2060 R⁸⁰ G²⁴ 2061 R⁸¹ G²¹ 2062 R⁸¹ G²² 2063 R⁸¹ G²³ 2064 R⁸¹ G²⁴ 2065 R⁸² G²¹ 2066 R⁸² G²² 2067 R⁸² G²³ 2068 R⁸² G²⁴ 2069 R⁸³ G²¹ 2070 R⁸³ G²² 2071 R⁸³ G²³ 2072 R⁸³ G²⁴ 2073 R⁸⁴ G²¹ 2074 R⁸⁴ G²² 2075 R⁸⁴ G²³ 2076 R⁸⁴ G²⁴ 2077 R⁸⁵ G²¹ 2078 R⁸⁵ G²² 2079 R⁸⁵ G²³ 2080 R⁸⁵ G²⁴ 2081 R⁸⁶ G²¹ 2082 R⁸⁶ G²² 2083 R⁸⁶ G²³ 2084 R⁸⁶ G²⁴ 2085 R⁸⁷ G²¹ 2086 R⁸⁷ G²² 2087 R⁸⁷ G²³ 2088 R⁸⁷ G²⁴ 2089 R¹ G²⁵ 2090 R¹ G²⁶ 2091 R¹ G²⁷ 2092 R¹ G²⁸ 2093 R² G²⁵ 2094 R² G²⁶ 2095 R² G²⁷ 2096 R² G²⁸ 2097 R³ G²⁵ 2098 R³ G²⁶ 2099 R³ G²⁷ 2100 R³ G²⁸ 2101 R⁴ G²⁵ 2102 R⁴ G²⁶ 2103 R⁴ G²⁷ 2104 R⁴ G²⁸ 2105 R⁵ G²⁵ 2106 R⁵ G²⁶ 2107 R⁵ G²⁷ 2108 R⁵ G²⁸ 2109 R⁶ G²⁵ 2110 R⁶ G²⁶ 2111 R⁶ G²⁷ 2112 R⁶ G²⁸ 2113 R⁷ G²⁵ 2114 R⁷ G²⁶ 2115 R⁷ G²⁷ 2116 R⁷ G²⁸ 2117 R⁸ G²⁵ 2118 R⁸ G²⁶ 2119 R⁸ G²⁷ 2120 R⁸ G²⁸ 2121 R⁹ G²⁵ 2122 R⁹ G²⁶ 2123 R⁹ G²⁷ 2124 R⁹ G²⁸ 2125 R¹⁰ G²⁵ 2126 R¹⁰ G²⁶ 2127 R¹⁰ G²⁷ 2128 R¹⁰ G²⁸ 2129 R¹¹ G²⁵ 2130 R¹¹ G²⁶ 2131 R¹¹ G²⁷ 2132 R¹¹ G²⁸ 2133 R¹² G²⁵ 2134 R¹² G²⁶ 2135 R¹² G²⁷ 2136 R¹² G²⁸ 2137 R¹³ G²⁵ 2138 R¹³ G²⁶ 2139 R¹³ G²⁷ 2140 R¹³ G²⁸ 2141 R¹⁴ G²⁵ 2142 R¹⁴ G²⁶ 2143 R¹⁴ G²⁷ 2144 R¹⁴ G²⁸ 2145 R¹⁵ G²⁵ 2146 R¹⁵ G²⁶ 2147 R¹⁵ G²⁷ 2148 R¹⁵ G²⁸ 2149 R¹⁶ G²⁵ 2150 R¹⁶ G²⁶ 2151 R¹⁶ G²⁷ 2152 R¹⁶ G²⁸ 2153 R¹⁷ G²⁵ 2154 R¹⁷ G²⁶ 2155 R¹⁷ G²⁷ 2156 R¹⁷ G²⁸ 2157 R¹⁸ G²⁵ 2158 R¹⁸ G²⁶ 2159 R¹⁸ G²⁷ 2160 R¹⁸ G²⁸ 2161 R¹⁹ G²⁵ 2162 R¹⁹ G²⁶ 2163 R¹⁹ G²⁷ 2164 R¹⁹ G²⁸ 2165 R²⁰ G²⁵ 2166 R²⁰ G²⁶ 2167 R²⁰ G²⁷ 2168 R²⁰ G²⁸ 2169 R²¹ G²⁵ 2170 R²¹ G²⁶ 2171 R²¹ G²⁷ 2172 R²¹ G²⁸ 2173 R²² G²⁵ 2174 R²² G²⁶ 2175 R²² G²⁷ 2176 R²² G²⁸ 2177 R²³ G²⁵ 2178 R²³ G²⁶ 2179 R²³ G²⁷ 2180 R²³ G²⁸ 2181 R²⁴ G²⁵ 2182 R²⁴ G²⁶ 2183 R²⁴ G²⁷ 2184 R²⁴ G²⁸ 2185 R²⁵ G²⁵ 2186 R²⁵ G²⁶ 2187 R²⁵ G²⁷ 2188 R²⁵ G²⁸ 2189 R²⁶ G²⁵ 2190 R²⁶ G²⁶ 2191 R²⁶ G²⁷ 2192 R²⁶ G²⁸ 2193 R²⁷ G²⁵ 2194 R²⁷ G²⁶ 2195 R²⁷ G²⁷ 2196 R²⁷ G²⁸ 2197 R²⁸ G²⁵ 2198 R²⁸ G²⁶ 2199 R²⁸ G²⁷ 2200 R²⁸ G²⁸ 2201 R²⁹ G²⁵ 2202 R²⁹ G²⁶ 2203 R²⁹ G²⁷ 2204 R²⁹ G²⁸ 2205 R³⁰ G²⁵ 2206 R³⁰ G²⁶ 2207 R³⁰ G²⁷ 2208 R³⁰ G²⁸ 2209 R³¹ G²⁵ 2210 R³¹ G²⁶ 2211 R³¹ G²⁷ 2212 R³¹ G²⁸ 2213 R³² G²⁵ 2214 R³² G²⁶ 2215 R³² G²⁷ 2216 R³² G²⁸ 2217 R³³ G²⁵ 2218 R³³ G²⁶ 2219 R³³ G²⁷ 2220 R³³ G²⁸ 2221 R³⁴ G²⁵ 2222 R³⁴ G²⁶ 2223 R³⁴ G²⁷ 2224 R³⁴ G²⁸ 2225 R³⁵ G²⁵ 2226 R³⁵ G²⁶ 2227 R³⁵ G²⁷ 2228 R³⁵ G²⁸ 2229 R³⁶ G²⁵ 2230 R³⁶ G²⁶ 2231 R³⁶ G²⁷ 2232 R³⁶ G²⁸ 2233 R³⁷ G²⁵ 2234 R³⁷ G²⁶ 2235 R³⁷ G²⁷ 2236 R³⁷ G²⁸ 2237 R³⁸ G²⁵ 2238 R³⁸ G²⁶ 2239 R³⁸ G²⁷ 2240 R³⁸ G²⁸ 2241 R³⁹ G²⁵ 2242 R³⁹ G²⁶ 2243 R³⁹ G²⁷ 2244 R³⁹ G²⁸ 2245 R⁴⁰ G²⁵ 2246 R⁴⁰ G²⁶ 2247 R⁴⁰ G²⁷ 2248 R⁴⁰ G²⁸ 2249 R⁴¹ G²⁵ 2250 R⁴¹ G²⁶ 2251 R⁴¹ G²⁷ 2252 R⁴¹ G²⁸ 2253 R⁴² G²⁵ 2254 R⁴² G²⁶ 2255 R⁴² G²⁷ 2256 R⁴² G²⁸ 2257 R⁴³ G²⁵ 2258 R⁴³ G²⁶ 2259 R⁴³ G²⁷ 2260 R⁴³ G²⁸ 2261 R⁴⁴ G²⁵ 2262 R⁴⁴ G²⁶ 2263 R⁴⁴ G²⁷ 2264 R⁴⁴ G²⁸ 2265 R⁴⁵ G²⁵ 2266 R⁴⁵ G²⁶ 2267 R⁴⁵ G²⁷ 2268 R⁴⁵ G²⁸ 2269 R⁴⁶ G²⁵ 2270 R⁴⁶ G²⁶ 2271 R⁴⁶ G²⁷ 2272 R⁴⁶ G²⁸ 2273 R⁴⁷ G²⁵ 2274 R⁴⁷ G²⁶ 2275 R⁴⁷ G²⁷ 2276 R⁴⁷ G²⁸ 2277 R⁴⁸ G²⁵ 2278 R⁴⁸ G²⁶ 2279 R⁴⁸ G²⁷ 2280 R⁴⁸ G²⁸ 2281 R⁴⁹ G²⁵ 2282 R⁴⁹ G²⁶ 2283 R⁴⁹ G²⁷ 2284 R⁴⁹ G²⁸ 2285 R⁵⁰ G²⁵ 2286 R⁵⁰ G²⁶ 2287 R⁵⁰ G²⁷ 2288 R⁵⁰ G²⁸ 2289 R⁵¹ G²⁵ 2290 R⁵¹ G²⁶ 2291 R⁵¹ G²⁷ 2292 R⁵¹ G²⁸ 2293 R⁵² G²⁵ 2294 R⁵² G²⁶ 2295 R⁵² G²⁷ 2296 R⁵² G²⁸ 2297 R⁵³ G²⁵ 2298 R⁵³ G²⁶ 2299 R⁵³ G²⁷ 2300 R⁵³ G²⁸ 2301 R⁵⁴ G²⁵ 2302 R⁵⁴ G²⁶ 2303 R⁵⁴ G²⁷ 2304 R⁵⁴ G²⁸ 2305 R⁵⁵ G²⁵ 2306 R⁵⁵ G²⁶ 2307 R⁵⁵ G²⁷ 2308 R⁵⁵ G²⁸ 2309 R⁵⁶ G²⁵ 2310 R⁵⁶ G²⁶ 2311 R⁵⁶ G²⁷ 2312 R⁵⁶ G²⁸ 2313 R⁵⁷ G²⁵ 2314 R⁵⁷ G²⁶ 2315 R⁵⁷ G²⁷ 2316 R⁵⁷ 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R¹⁰ G²⁹ 2474 R¹⁰ G³⁰ 2475 R¹⁰ G³¹ 2476 R¹⁰ G³² 2477 R¹¹ G²⁹ 2478 R¹¹ G³⁰ 2479 R¹¹ G³¹ 2480 R¹¹ G³² 2481 R¹² G²⁹ 2482 R¹² G³⁰ 2483 R¹² G³¹ 2484 R¹² G³² 2485 R¹³ G²⁹ 2486 R¹³ G³⁰ 2487 R¹³ G³¹ 2488 R¹³ G³² 2489 R¹⁴ G²⁹ 2490 R¹⁴ G³⁰ 2491 R¹⁴ G³¹ 2492 R¹⁴ G³² 2493 R¹⁵ G²⁹ 2494 R¹⁵ G³⁰ 2495 R¹⁵ G³¹ 2496 R¹⁵ G³² 2497 R¹⁶ G²⁹ 2498 R¹⁶ G³⁰ 2499 R¹⁶ G³¹ 2500 R¹⁶ G³² 2501 R¹⁷ G²⁹ 2502 R¹⁷ G³⁰ 2503 R¹⁷ G³¹ 2504 R¹⁷ G³² 2505 R¹⁸ G²⁹ 2506 R¹⁸ G³⁰ 2507 R¹⁸ G³¹ 2508 R¹⁸ G³² 2509 R¹⁹ G²⁹ 2510 R¹⁹ G³⁰ 2511 R¹⁹ G³¹ 2512 R¹⁹ G³² 2513 R²⁰ G²⁹ 2514 R²⁰ G³⁰ 2515 R²⁰ G³¹ 2516 R²⁰ G³² 2517 R²¹ G²⁹ 2518 R²¹ G³⁰ 2519 R²¹ G³¹ 2520 R²¹ G³² 2521 R²² G²⁹ 2522 R²² G³⁰ 2523 R²² G³¹ 2524 R²² G³² 2525 R²³ G²⁹ 2526 R²³ G³⁰ 2527 R²³ G³¹ 2528 R²³ G³² 2529 R²⁴ G²⁹ 2530 R²⁴ G³⁰ 2531 R²⁴ G³¹ 2532 R²⁴ G³² 2533 R²⁵ G²⁹ 2534 R²⁵ G³⁰ 2535 R²⁵ G³¹ 2536 R²⁵ G³² 2537 R²⁶ G²⁹ 2538 R²⁶ G³⁰ 2539 R²⁶ G³¹ 2540 R²⁶ G³² 2541 R²⁷ G²⁹ 2542 R²⁷ G³⁰ 2543 R²⁷ G³¹ 2544 R²⁷ G³² 2545 R²⁸ G²⁹ 2546 R²⁸ G³⁰ 2547 R²⁸ G³¹ 2548 R²⁸ G³² 2549 R²⁹ G²⁹ 2550 R²⁹ G³⁰ 2551 R²⁹ G³¹ 2552 R²⁹ G³² 2553 R³⁰ G²⁹ 2554 R³⁰ G³⁰ 2555 R³⁰ G³¹ 2556 R³⁰ G³² 2557 R³¹ G²⁹ 2558 R³¹ G³⁰ 2559 R³¹ G³¹ 2560 R³¹ G³² 2561 R³² G²⁹ 2562 R³² G³⁰ 2563 R³² G³¹ 2564 R³² G³² 2565 R³³ G²⁹ 2566 R³³ G³⁰ 2567 R³³ G³¹ 2568 R³³ G³² 2569 R³⁴ G²⁹ 2570 R³⁴ G³⁰ 2571 R³⁴ G³¹ 2572 R³⁴ G³² 2573 R³⁵ G²⁹ 2574 R³⁵ G³⁰ 2575 R³⁵ G³¹ 2576 R³⁵ G³² 2577 R³⁶ G²⁹ 2578 R³⁶ G³⁰ 2579 R³⁶ G³¹ 2580 R³⁶ G³² 2581 R³⁷ G²⁹ 2582 R³⁷ G³⁰ 2583 R³⁷ G³¹ 2584 R³⁷ G³² 2585 R³⁸ G²⁹ 2586 R³⁸ G³⁰ 2587 R³⁸ G³¹ 2588 R³⁸ G³² 2589 R³⁹ G²⁹ 2590 R³⁹ G³⁰ 2591 R³⁹ G³¹ 2592 R³⁹ G³² 2593 R⁴⁰ G²⁹ 2594 R⁴⁰ G³⁰ 2595 R⁴⁰ G³¹ 2596 R⁴⁰ G³² 2597 R⁴¹ G²⁹ 2598 R⁴¹ G³⁰ 2599 R⁴¹ G³¹ 2600 R⁴¹ G³² 2601 R⁴² G²⁹ 2602 R⁴² G³⁰ 2603 R⁴² G³¹ 2604 R⁴² G³² 2605 R⁴³ G²⁹ 2606 R⁴³ G³⁰ 2607 R⁴³ G³¹ 2608 R⁴³ G³² 2609 R⁴⁴ G²⁹ 2610 R⁴⁴ G³⁰ 2611 R⁴⁴ G³¹ 2612 R⁴⁴ G³² 2613 R⁴⁵ G²⁹ 2614 R⁴⁵ G³⁰ 2615 R⁴⁵ G³¹ 2616 R⁴⁵ G³² 2617 R⁴⁶ G²⁹ 2618 R⁴⁶ G³⁰ 2619 R⁴⁶ G³¹ 2620 R⁴⁶ G³² 2621 R⁴⁷ G²⁹ 2622 R⁴⁷ G³⁰ 2623 R⁴⁷ G³¹ 2624 R⁴⁷ G³² 2625 R⁴⁸ G²⁹ 2626 R⁴⁸ G³⁰ 2627 R⁴⁸ G³¹ 2628 R⁴⁸ G³² 2629 R⁴⁹ G²⁹ 2630 R⁴⁹ G³⁰ 2631 R⁴⁹ G³¹ 2632 R⁴⁹ G³² 2633 R⁵⁰ G²⁹ 2634 R⁵⁰ G³⁰ 2635 R⁵⁰ G³¹ 2636 R⁵⁰ G³² 2637 R⁵¹ G²⁹ 2638 R⁵¹ G³⁰ 2639 R⁵¹ G³¹ 2640 R⁵¹ G³² 2641 R⁵² G²⁹ 2642 R⁵² G³⁰ 2643 R⁵² G³¹ 2644 R⁵² G³² 2645 R⁵³ G²⁹ 2646 R⁵³ G³⁰ 2647 R⁵³ G³¹ 2648 R⁵³ G³² 2649 R⁵⁴ G²⁹ 2650 R⁵⁴ G³⁰ 2651 R⁵⁴ G³¹ 2652 R⁵⁴ G³² 2653 R⁵⁵ G²⁹ 2654 R⁵⁵ G³⁰ 2655 R⁵⁵ G³¹ 2656 R⁵⁵ G³² 2657 R⁵⁶ G²⁹ 2658 R⁵⁶ G³⁰ 2659 R⁵⁶ G³¹ 2660 R⁵⁶ G³² 2661 R⁵⁷ G²⁹ 2662 R⁵⁷ G³⁰ 2663 R⁵⁷ G³¹ 2664 R⁵⁷ G³² 2665 R⁵⁸ G²⁹ 2666 R⁵⁸ G³⁰ 2667 R⁵⁸ G³¹ 2668 R⁵⁸ G³² 2669 R⁵⁹ G²⁹ 2670 R⁵⁹ G³⁰ 2671 R⁵⁹ G³¹ 2672 R⁵⁹ G³² 2673 R⁶⁰ G²⁹ 2674 R⁶⁰ G³⁰ 2675 R⁶⁰ G³¹ 2676 R⁶⁰ G³² 2677 R⁶¹ G²⁹ 2678 R⁶¹ G³⁰ 2679 R⁶¹ G³¹ 2680 R⁶¹ G³² 2681 R⁶² G²⁹ 2682 R⁶² G³⁰ 2683 R⁶² G³¹ 2684 R⁶² G³² 2685 R⁶³ G²⁹ 2686 R⁶³ G³⁰ 2687 R⁶³ G³¹ 2688 R⁶³ G³² 2689 R⁶⁴ G²⁹ 2690 R⁶⁴ G³⁰ 2691 R⁶⁴ G³¹ 2692 R⁶⁴ G³² 2693 R⁶⁵ G²⁹ 2694 R⁶⁵ G³⁰ 2695 R⁶⁵ G³¹ 2696 R⁶⁵ G³² 2697 R⁶⁶ G²⁹ 2698 R⁶⁶ G³⁰ 2699 R⁶⁶ G³¹ 2700 R⁶⁶ G³² 2701 R⁶⁷ G²⁹ 2702 R⁶⁷ G³⁰ 2703 R⁶⁷ G³¹ 2704 R⁶⁷ G³² 2705 R⁶⁸ G²⁹ 2706 R⁶⁸ G³⁰ 2707 R⁶⁸ G³¹ 2708 R⁶⁸ G³² 2709 R⁶⁹ G²⁹ 2710 R⁶⁹ G³⁰ 2711 R⁶⁹ G³¹ 2712 R⁶⁹ G³² 2713 R⁷⁰ G²⁹ 2714 R⁷⁰ G³⁰ 2715 R⁷⁰ G³¹ 2716 R⁷⁰ G³² 2717 R⁷¹ G²⁹ 2718 R⁷¹ G³⁰ 2719 R⁷¹ G³¹ 2720 R⁷¹ G³² 2721 R⁷² G²⁹ 2722 R⁷² G³⁰ 2723 R⁷² G³¹ 2724 R⁷² G³² 2725 R⁷³ G²⁹ 2726 R⁷³ G³⁰ 2727 R⁷³ G³¹ 2728 R⁷³ G³² 2729 R⁷⁴ G²⁹ 2730 R⁷⁴ G³⁰ 2731 R⁷⁴ G³¹ 2732 R⁷⁴ G³² 2733 R⁷⁵ G²⁹ 2734 R⁷⁵ G³⁰ 2735 R⁷⁵ G³¹ 2736 R⁷⁵ G³² 2737 R⁷⁶ G²⁹ 2738 R⁷⁶ G³⁰ 2739 R⁷⁶ G³¹ 2740 R⁷⁶ G³² 2741 R⁷⁷ G²⁹ 2742 R⁷⁷ G³⁰ 2743 R⁷⁷ G³¹ 2744 R⁷⁷ G³² 2745 R⁷⁸ G²⁹ 2746 R⁷⁸ G³⁰ 2747 R⁷⁸ G³¹ 2748 R⁷⁸ G³² 2749 R⁷⁹ G²⁹ 2750 R⁷⁹ G³⁰ 2751 R⁷⁹ G³¹ 2752 R⁷⁹ G³² 2753 R⁸⁰ G²⁹ 2754 R⁸⁰ G³⁰ 2755 R⁸⁰ G³¹ 2756 R⁸⁰ G³² 2757 R⁸¹ G²⁹ 2758 R⁸¹ G³⁰ 2759 R⁸¹ G³¹ 2760 R⁸¹ G³² 2761 R⁸² G²⁹ 2762 R⁸² G³⁰ 2763 R⁸² G³¹ 2764 R⁸² G³² 2765 R⁸³ G²⁹ 2766 R⁸³ G³⁰ 2767 R⁸³ G³¹ 2768 R⁸³ G³² 2769 R⁸⁴ G²⁹ 2770 R⁸⁴ G³⁰ 2771 R⁸⁴ G³¹ 2772 R⁸⁴ G³² 2773 R⁸⁵ G²⁹ 2774 R⁸⁵ G³⁰ 2775 R⁸⁵ G³¹ 2776 R⁸⁵ G³² 2777 R⁸⁶ G²⁹ 2778 R⁸⁶ G³⁰ 2779 R⁸⁶ G³¹ 2780 R⁸⁶ G³² 2781 R⁸⁷ G²⁹ 2782 R⁸⁷ G³⁰ 2783 R⁸⁷ G³¹ 2784 R⁸⁷ G³² 2785 R¹ G³³ 2786 R¹ G³⁴ 2787 R¹ G³⁵ 2788 R¹ G³⁶ 2789 R² G³³ 2790 R² G³⁴ 2791 R² G³⁵ 2792 R² G³⁶ 2793 R³ G³³ 2794 R³ G³⁴ 2795 R³ G³⁵ 2796 R³ G³⁶ 2797 R⁴ G³³ 2798 R⁴ G³⁴ 2799 R⁴ G³⁵ 2800 R⁴ G³⁶ 2801 R⁵ G³³ 2802 R⁵ G³⁴ 2803 R⁵ G³⁵ 2804 R⁵ G³⁶ 2805 R⁶ G³³ 2806 R⁶ G³⁴ 2807 R⁶ G³⁵ 2808 R⁶ G³⁶ 2809 R⁷ G³³ 2810 R⁷ G³⁴ 2811 R⁷ G³⁵ 2812 R⁷ G³⁶ 2813 R⁸ G³³ 2814 R⁸ G³⁴ 2815 R⁸ G³⁵ 2816 R⁸ G³⁶ 2817 R⁹ G³³ 2818 R⁹ G³⁴ 2819 R⁹ G³⁵ 2820 R⁹ G³⁶ 2821 R¹⁰ G³³ 2822 R¹⁰ G³⁴ 2823 R¹⁰ G³⁵ 2824 R¹⁰ G³⁶ 2825 R¹¹ G³³ 2826 R¹¹ G³⁴ 2827 R¹¹ G³⁵ 2828 R¹¹ G³⁶ 2829 R¹² G³³ 2830 R¹² G³⁴ 2831 R¹² G³⁵ 2832 R¹² G³⁶ 2833 R¹³ G³³ 2834 R¹³ G³⁴ 2835 R¹³ G³⁵ 2836 R¹³ G³⁶ 2837 R¹⁴ G³³ 2838 R¹⁴ G³⁴ 2839 R¹⁴ G³⁵ 2840 R¹⁴ G³⁶ 2841 R¹⁵ G³³ 2842 R¹⁵ G³⁴ 2843 R¹⁵ G³⁵ 2844 R¹⁵ G³⁶ 2845 R¹⁶ G³³ 2846 R¹⁶ G³⁴ 2847 R¹⁶ G³⁵ 2848 R¹⁶ G³⁶ 2849 R¹⁷ G³³ 2850 R¹⁷ G³⁴ 2851 R¹⁷ G³⁵ 2852 R¹⁷ G³⁶ 2853 R¹⁸ G³³ 2854 R¹⁸ G³⁴ 2855 R¹⁸ G³⁵ 2856 R¹⁸ G³⁶ 2857 R¹⁹ G³³ 2858 R¹⁹ G³⁴ 2859 R¹⁹ G³⁵ 2860 R¹⁹ G³⁶ 2861 R²⁰ G³³ 2862 R²⁰ G³⁴ 2863 R²⁰ G³⁵ 2864 R²⁰ G³⁶ 2865 R²¹ G³³ 2866 R²¹ G³⁴ 2867 R²¹ G³⁵ 2868 R²¹ G³⁶ 2869 R²² G³³ 2870 R²² G³⁴ 2871 R²² G³⁵ 2872 R²² G³⁶ 2873 R²³ G³³ 2874 R²³ G³⁴ 2875 R²³ G³⁵ 2876 R²³ G³⁶ 2877 R²⁴ G³³ 2878 R²⁴ G³⁴ 2879 R²⁴ G³⁵ 2880 R²⁴ G³⁶ 2881 R²⁵ G³³ 2882 R²⁵ G³⁴ 2883 R²⁵ G³⁵ 2884 R²⁵ G³⁶ 2885 R²⁶ G³³ 2886 R²⁶ G³⁴ 2887 R²⁶ G³⁵ 2888 R²⁶ G³⁶ 2889 R²⁷ G³³ 2890 R²⁷ G³⁴ 2891 R²⁷ G³⁵ 2892 R²⁷ G³⁶ 2893 R²⁸ G³³ 2894 R²⁸ G³⁴ 2895 R²⁸ G³⁵ 2896 R²⁸ G³⁶ 2897 R²⁹ G³³ 2898 R²⁹ G³⁴ 2899 R²⁹ G³⁵ 2900 R²⁹ G³⁶ 2901 R³⁰ G³³ 2902 R³⁰ G³⁴ 2903 R³⁰ G³⁵ 2904 R³⁰ G³⁶ 2905 R³¹ G³³ 2906 R³¹ G³⁴ 2907 R³¹ G³⁵ 2908 R³¹ G³⁶ 2909 R³² G³³ 2910 R³² G³⁴ 2911 R³² G³⁵ 2912 R³² G³⁶ 2913 R³³ G³³ 2914 R³³ G³⁴ 2915 R³³ G³⁵ 2916 R³³ G³⁶ 2917 R³⁴ G³³ 2918 R³⁴ G³⁴ 2919 R³⁴ G³⁵ 2920 R³⁴ G³⁶ 2921 R³⁵ G³³ 2922 R³⁵ G³⁴ 2923 R³⁵ G³⁵ 2924 R³⁵ G³⁶ 2925 R³⁶ G³³ 2926 R³⁶ G³⁴ 2927 R³⁶ G³⁵ 2928 R³⁶ G³⁶ 2929 R³⁷ G³³ 2930 R³⁷ G³⁴ 2931 R³⁷ G³⁵ 2932 R³⁷ G³⁶ 2933 R³⁸ G³³ 2934 R³⁸ G³⁴ 2935 R³⁸ G³⁵ 2936 R³⁸ G³⁶ 2937 R³⁹ G³³ 2938 R³⁹ G³⁴ 2939 R³⁹ G³⁵ 2940 R³⁹ G³⁶ 2941 R⁴⁰ G³³ 2942 R⁴⁰ G³⁴ 2943 R⁴⁰ G³⁵ 2944 R⁴⁰ G³⁶ 2945 R⁴¹ G³³ 2946 R⁴¹ G³⁴ 2947 R⁴¹ G³⁵ 2948 R⁴¹ G³⁶ 2949 R⁴² G³³ 2950 R⁴² G³⁴ 2951 R⁴² G³⁵ 2952 R⁴² G³⁶ 2953 R⁴³ G³³ 2954 R⁴³ G³⁴ 2955 R⁴³ G³⁵ 2956 R⁴³ G³⁶ 2957 R⁴⁴ G³³ 2958 R⁴⁴ G³⁴ 2959 R⁴⁴ G³⁵ 2960 R⁴⁴ G³⁶ 2961 R⁴⁵ G³³ 2962 R⁴⁵ G³⁴ 2963 R⁴⁵ G³⁵ 2964 R⁴⁵ G³⁶ 2965 R⁴⁶ G³³ 2966 R⁴⁶ G³⁴ 2967 R⁴⁶ G³⁵ 2968 R⁴⁶ G³⁶ 2969 R⁴⁷ G³³ 2970 R⁴⁷ G³⁴ 2971 R⁴⁷ G³⁵ 2972 R⁴⁷ G³⁶ 2973 R⁴⁸ G³³ 2974 R⁴⁸ G³⁴ 2975 R⁴⁸ G³⁵ 2976 R⁴⁸ G³⁶ 2977 R⁴⁹ G³³ 2978 R⁴⁹ G³⁴ 2979 R⁴⁹ G³⁵ 2980 R⁴⁹ G³⁶ 2981 R⁵⁰ G³³ 2982 R⁵⁰ G³⁴ 2983 R⁵⁰ G³⁵ 2984 R⁵⁰ G³⁶ 2985 R⁵¹ G³³ 2986 R⁵¹ G³⁴ 2987 R⁵¹ G³⁵ 2988 R⁵¹ G³⁶ 2989 R⁵² G³³ 2990 R⁵² G³⁴ 2991 R⁵² G³⁵ 2992 R⁵² G³⁶ 2993 R⁵³ G³³ 2994 R⁵³ G³⁴ 2995 R⁵³ G³⁵ 2996 R⁵³ G³⁶ 2997 R⁵⁴ G³³ 2998 R⁵⁴ G³⁴ 2999 R⁵⁴ G³⁵ 3000 R⁵⁴ G³⁶ 3001 R⁵⁵ G³³ 3002 R⁵⁵ G³⁴ 3003 R⁵⁵ G³⁵ 3004 R⁵⁵ G³⁶ 3005 R⁵⁶ G³³ 3006 R⁵⁶ G³⁴ 3007 R⁵⁶ G³⁵ 3008 R⁵⁶ G³⁶ 3009 R⁵⁷ G³³ 3010 R⁵⁷ G³⁴ 3011 R⁵⁷ G³⁵ 3012 R⁵⁷ G³⁶ 3013 R⁵⁸ G³³ 3014 R⁵⁸ G³⁴ 3015 R⁵⁸ G³⁵ 3016 R⁵⁸ G³⁶ 3017 R⁵⁹ G³³ 3018 R⁵⁹ G³⁴ 3019 R⁵⁹ G³⁵ 3020 R⁵⁹ G³⁶ 3021 R⁶⁰ G³³ 3022 R⁶⁰ G³⁴ 3023 R⁶⁰ G³⁵ 3024 R⁶⁰ G³⁶ 3025 R⁶¹ G³³ 3026 R⁶¹ G³⁴ 3027 R⁶¹ G³⁵ 3028 R⁶¹ G³⁶ 3029 R⁶² G³³ 3030 R⁶² G³⁴ 3031 R⁶² G³⁵ 3032 R⁶² G³⁶ 3033 R⁶³ G³³ 3034 R⁶³ G³⁴ 3035 R⁶³ G³⁵ 3036 R⁶³ G³⁶ 3037 R⁶⁴ G³³ 3038 R⁶⁴ G³⁴ 3039 R⁶⁴ G³⁵ 3040 R⁶⁴ G³⁶ 3041 R⁶⁵ G³³ 3042 R⁶⁵ G³⁴ 3043 R⁶⁵ G³⁵ 3044 R⁶⁵ G³⁶ 3045 R⁶⁶ G³³ 3046 R⁶⁶ G³⁴ 3047 R⁶⁶ G³⁵ 3048 R⁶⁶ G³⁶ 3049 R⁶⁷ G³³ 3050 R⁶⁷ G³⁴ 3051 R⁶⁷ G³⁵ 3052 R⁶⁷ G³⁶ 3053 R⁶⁸ G³³ 3054 R⁶⁸ G³⁴ 3055 R⁶⁸ G³⁵ 3056 R⁶⁸ G³⁶ 3057 R⁶⁹ G³³ 3058 R⁶⁹ G³⁴ 3059 R⁶⁹ G³⁵ 3060 R⁶⁹ G³⁶ 3061 R⁷⁰ G³³ 3062 R⁷⁰ G³⁴ 3063 R⁷⁰ G³⁵ 3064 R⁷⁰ G³⁶ 3065 R⁷¹ G³³ 3066 R⁷¹ G³⁴ 3067 R⁷¹ G³⁵ 3068 R⁷¹ G³⁶ 3069 R⁷² G³³ 3070 R⁷² G³⁴ 3071 R⁷² G³⁵ 3072 R⁷² G³⁶ 3073 R⁷³ G³³ 3074 R⁷³ G³⁴ 3075 R⁷³ G³⁵ 3076 R⁷³ G³⁶ 3077 R⁷⁴ G³³ 3078 R⁷⁴ G³⁴ 3079 R⁷⁴ G³⁵ 3080 R⁷⁴ G³⁶ 3081 R⁷⁵ G³³ 3082 R⁷⁵ G³⁴ 3083 R⁷⁵ G³⁵ 3084 R⁷⁵ G³⁶ 3085 R⁷⁶ G³³ 3086 R⁷⁶ G³⁴ 3087 R⁷⁶ G³⁵ 3088 R⁷⁶ G³⁶ 3089 R⁷⁷ G³³ 3090 R⁷⁷ G³⁴ 3091 R⁷⁷ G³⁵ 3092 R⁷⁷ G³⁶ 3093 R⁷⁸ G³³ 3094 R⁷⁸ G³⁴ 3095 R⁷⁸ G³⁵ 3096 R⁷⁸ G³⁶ 3097 R⁷⁹ G³³ 3098 R⁷⁹ G³⁴ 3099 R⁷⁹ G³⁵ 3100 R⁷⁹ G³⁶ 3101 R⁸⁰ G³³ 3102 R⁸⁰ G³⁴ 3103 R⁸⁰ G³⁵ 3104 R⁸⁰ G³⁶ 3105 R⁸¹ G³³ 3106 R⁸¹ G³⁴ 3107 R⁸¹ G³⁵ 3108 R⁸¹ G³⁶ 3109 R⁸² G³³ 3110 R⁸² G³⁴ 3111 R⁸² G³⁵ 3112 R⁸² G³⁶ 3113 R⁸³ G³³ 3114 R⁸³ G³⁴ 3115 R⁸³ G³⁵ 3116 R⁸³ G³⁶ 3117 R⁸⁴ G³³ 3118 R⁸⁴ G³⁴ 3119 R⁸⁴ G³⁵ 3120 R⁸⁴ G³⁶ 3121 R⁸⁵ G³³ 3122 R⁸⁵ G³⁴ 3123 R⁸⁵ G³⁵ 3124 R⁸⁵ G³⁶ 3125 R⁸⁶ G³³ 3126 R⁸⁶ G³⁴ 3127 R⁸⁶ G³⁵ 3128 R⁸⁶ G³⁶ 3129 R⁸⁷ G³³ 3130 R⁸⁷ G³⁴ 3131 R⁸⁷ G³⁵ 3132 R⁸⁷ G³⁶ 3133 R¹ G³⁷ 3134 R¹ G³⁸ 3135 R¹ G³⁹ 3136 R¹ G⁴⁰ 3137 R² G³⁷ 3138 R² G³⁸ 3139 R² G³⁹ 3140 R² G⁴⁰ 3141 R³ G³⁷ 3142 R³ G³⁸ 3143 R³ G³⁹ 3144 R³ G⁴⁰ 3145 R⁴ G³⁷ 3146 R⁴ G³⁸ 3147 R⁴ G³⁹ 3148 R⁴ G⁴⁰ 3149 R⁵ G³⁷ 3150 R⁵ G³⁸ 3151 R⁵ G³⁹ 3152 R⁵ G⁴⁰ 3153 R⁶ G³⁷ 3154 R⁶ G³⁸ 3155 R⁶ G³⁹ 3156 R⁶ G⁴⁰ 3157 R⁷ G³⁷ 3158 R⁷ G³⁸ 3159 R⁷ G³⁹ 3160 R⁷ G⁴⁰ 3161 R⁸ G³⁷ 3162 R⁸ G³⁸ 3163 R⁸ G³⁹ 3164 R⁸ G⁴⁰ 3165 R⁹ G³⁷ 3166 R⁹ G³⁸ 3167 R⁹ G³⁹ 3168 R⁹ G⁴⁰ 3169 R¹⁰ G³⁷ 3170 R¹⁰ G³⁸ 3171 R¹⁰ G³⁹ 3172 R¹⁰ G⁴⁰ 3173 R¹¹ G³⁷ 3174 R¹¹ G³⁸ 3175 R¹¹ G³⁹ 3176 R¹¹ G⁴⁰ 3177 R¹² G³⁷ 3178 R¹² G³⁸ 3179 R¹² G³⁹ 3180 R¹² G⁴⁰ 3181 R¹³ G³⁷ 3182 R¹³ G³⁸ 3183 R¹³ G³⁹ 3184 R¹³ G⁴⁰ 3185 R¹⁴ G³⁷ 3186 R¹⁴ G³⁸ 3187 R¹⁴ G³⁹ 3188 R¹⁴ G⁴⁰ 3189 R¹⁵ G³⁷ 3190 R¹⁵ G³⁸ 3191 R¹⁵ G³⁹ 3192 R¹⁵ G⁴⁰ 3193 R¹⁶ G³⁷ 3194 R¹⁶ G³⁸ 3195 R¹⁶ G³⁹ 3196 R¹⁶ G⁴⁰ 3197 R¹⁷ G³⁷ 3198 R¹⁷ G³⁸ 3199 R¹⁷ G³⁹ 3200 R¹⁷ G⁴⁰ 3201 R¹⁸ G³⁷ 3202 R¹⁸ G³⁸ 3203 R¹⁸ G³⁹ 3204 R¹⁸ G⁴⁰ 3205 R¹⁹ G³⁷ 3206 R¹⁹ G³⁸ 3207 R¹⁹ G³⁹ 3208 R¹⁹ G⁴⁰ 3209 R²⁰ G³⁷ 3210 R²⁰ G³⁸ 3211 R²⁰ G³⁹ 3212 R²⁰ G⁴⁰ 3213 R²¹ G³⁷ 3214 R²¹ G³⁸ 3215 R²¹ G³⁹ 3216 R²¹ G⁴⁰ 3217 R²² G³⁷ 3218 R²² G³⁸ 3219 R²² G³⁹ 3220 R²² G⁴⁰ 3221 R²³ G³⁷ 3222 R²³ G³⁸ 3223 R²³ G³⁹ 3224 R²³ G⁴⁰ 3225 R²⁴ G³⁷ 3226 R²⁴ G³⁸ 3227 R²⁴ G³⁹ 3228 R²⁴ G⁴⁰ 3229 R²⁵ G³⁷ 3230 R²⁵ G³⁸ 3231 R²⁵ G³⁹ 3232 R²⁵ G⁴⁰ 3233 R²⁶ G³⁷ 3234 R²⁶ G³⁸ 3235 R²⁶ G³⁹ 3236 R²⁶ G⁴⁰ 3237 R²⁷ G³⁷ 3238 R²⁷ G³⁸ 3239 R²⁷ G³⁹ 3240 R²⁷ G⁴⁰ 3241 R²⁸ G³⁷ 3242 R²⁸ G³⁸ 3243 R²⁸ G³⁹ 3244 R²⁸ G⁴⁰ 3245 R²⁹ G³⁷ 3246 R²⁹ G³⁸ 3247 R²⁹ G³⁹ 3248 R²⁹ G⁴⁰ 3249 R³⁰ G³⁷ 3250 R³⁰ G³⁸ 3251 R³⁰ G³⁹ 3252 R³⁰ G⁴⁰ 3253 R³¹ G³⁷ 3254 R³¹ G³⁸ 3255 R³¹ G³⁹ 3256 R³¹ G⁴⁰ 3257 R³² G³⁷ 3258 R³² G³⁸ 3259 R³² G³⁹ 3260 R³² G⁴⁰ 3261 R³³ G³⁷ 3262 R³³ G³⁸ 3263 R³³ G³⁹ 3264 R³³ G⁴⁰ 3265 R³⁴ G³⁷ 3266 R³⁴ G³⁸ 3267 R³⁴ G³⁹ 3268 R³⁴ G⁴⁰ 3269 R³⁵ G³⁷ 3270 R³⁵ G³⁸ 3271 R³⁵ G³⁹ 3272 R³⁵ G⁴⁰ 3273 R³⁶ G³⁷ 3274 R³⁶ G³⁸ 3275 R³⁶ G³⁹ 3276 R³⁶ G⁴⁰ 3277 R³⁷ G³⁷ 3278 R³⁷ G³⁸ 3279 R³⁷ G³⁹ 3280 R³⁷ G⁴⁰ 3281 R³⁸ G³⁷ 3282 R³⁸ G³⁸ 3283 R³⁸ G³⁹ 3284 R³⁸ G⁴⁰ 3285 R³⁹ G³⁷ 3286 R³⁹ G³⁸ 3287 R³⁹ G³⁹ 3288 R³⁹ G⁴⁰ 3289 R⁴⁰ G³⁷ 3290 R⁴⁰ G³⁸ 3291 R⁴⁰ G³⁹ 3292 R⁴⁰ G⁴⁰ 3293 R⁴¹ G³⁷ 3294 R⁴¹ G³⁸ 3295 R⁴¹ G³⁹ 3296 R⁴¹ G⁴⁰ 3297 R⁴² G³⁷ 3298 R⁴² G³⁸ 3299 R⁴² G³⁹ 3300 R⁴² G⁴⁰ 3301 R⁴³ G³⁷ 3302 R⁴³ G³⁸ 3303 R⁴³ G³⁹ 3304 R⁴³ G⁴⁰ 3305 R⁴⁴ G³⁷ 3306 R⁴⁴ G³⁸ 3307 R⁴⁴ G³⁹ 3308 R⁴⁴ G⁴⁰ 3309 R⁴⁵ G³⁷ 3310 R⁴⁵ G³⁸ 3311 R⁴⁵ G³⁹ 3312 R⁴⁵ G⁴⁰ 3313 R⁴⁶ G³⁷ 3314 R⁴⁶ G³⁸ 3315 R⁴⁶ G³⁹ 3316 R⁴⁶ G⁴⁰ 3317 R⁴⁷ G³⁷ 3318 R⁴⁷ G³⁸ 3319 R⁴⁷ G³⁹ 3320 R⁴⁷ G⁴⁰ 3321 R⁴⁸ G³⁷ 3322 R⁴⁸ G³⁸ 3323 R⁴⁸ G³⁹ 3324 R⁴⁸ G⁴⁰ 3325 R⁴⁹ G³⁷ 3326 R⁴⁹ G³⁸ 3327 R⁴⁹ G³⁹ 3328 R⁴⁹ G⁴⁰ 3329 R⁵⁰ G³⁷ 3330 R⁵⁰ G³⁸ 3331 R⁵⁰ G³⁹ 3332 R⁵⁰ G⁴⁰ 3333 R⁵¹ G³⁷ 3334 R⁵¹ G³⁸ 3335 R⁵¹ G³⁹ 3336 R⁵¹ G⁴⁰ 3337 R⁵² G³⁷ 3338 R⁵² G³⁸ 3339 R⁵² G³⁹ 3340 R⁵² G⁴⁰ 3341 R⁵³ G³⁷ 3342 R⁵³ G³⁸ 3343 R⁵³ G³⁹ 3344 R⁵³ G⁴⁰ 3345 R⁵⁴ G³⁷ 3346 R⁵⁴ G³⁸ 3347 R⁵⁴ G³⁹ 3348 R⁵⁴ G⁴⁰ 3349 R⁵⁵ G³⁷ 3350 R⁵⁵ G³⁸ 3351 R⁵⁵ G³⁹ 3352 R⁵⁵ G⁴⁰ 3353 R⁵⁶ G³⁷ 3354 R⁵⁶ G³⁸ 3355 R⁵⁶ G³⁹ 3356 R⁵⁶ G⁴⁰ 3357 R⁵⁷ G³⁷ 3358 R⁵⁷ G³⁸ 3359 R⁵⁷ G³⁹ 3360 R⁵⁷ G⁴⁰ 3361 R⁵⁸ G³⁷ 3362 R⁵⁸ G³⁸ 3363 R⁵⁸ G³⁹ 3364 R⁵⁸ G⁴⁰ 3365 R⁵⁹ G³⁷ 3366 R⁵⁹ G³⁸ 3367 R⁵⁹ G³⁹ 3368 R⁵⁹ G⁴⁰ 3369 R⁶⁰ G³⁷ 3370 R⁶⁰ G³⁸ 3371 R⁶⁰ G³⁹ 3372 R⁶⁰ G⁴⁰ 3373 R⁶¹ G³⁷ 3374 R⁶¹ G³⁸ 3375 R⁶¹ G³⁹ 3376 R⁶¹ G⁴⁰ 3377 R⁶² G³⁷ 3378 R⁶² G³⁸ 3379 R⁶² G³⁹ 3380 R⁶² G⁴⁰ 3381 R⁶³ G³⁷ 3382 R⁶³ G³⁸ 3383 R⁶³ G³⁹ 3384 R⁶³ G⁴⁰ 3385 R⁶⁴ G³⁷ 3386 R⁶⁴ G³⁸ 3387 R⁶⁴ G³⁹ 3388 R⁶⁴ G⁴⁰ 3389 R⁶⁵ G³⁷ 3390 R⁶⁵ G³⁸ 3391 R⁶⁵ G³⁹ 3392 R⁶⁵ G⁴⁰ 3393 R⁶⁶ G³⁷ 3394 R⁶⁶ G³⁸ 3395 R⁶⁶ G³⁹ 3396 R⁶⁶ G⁴⁰ 3397 R⁶⁷ G³⁷ 3398 R⁶⁷ G³⁸ 3399 R⁶⁷ G³⁹ 3400 R⁶⁷ G⁴⁰ 3401 R⁶⁸ G³⁷ 3402 R⁶⁸ G³⁸ 3403 R⁶⁸ G³⁹ 3404 R⁶⁸ G⁴⁰ 3405 R⁶⁹ G³⁷ 3406 R⁶⁹ G³⁸ 3407 R⁶⁹ G³⁹ 3408 R⁶⁹ G⁴⁰ 3409 R⁷⁰ G³⁷ 3410 R⁷⁰ G³⁸ 3411 R⁷⁰ G³⁹ 3412 R⁷⁰ G⁴⁰ 3413 R⁷¹ G³⁷ 3414 R⁷¹ G³⁸ 3415 R⁷¹ G³⁹ 3416 R⁷¹ G⁴⁰ 3417 R⁷² G³⁷ 3418 R⁷² G³⁸ 3419 R⁷² G³⁹ 3420 R⁷² G⁴⁰ 3421 R⁷³ G³⁷ 3422 R⁷³ G³⁸ 3423 R⁷³ G³⁹ 3424 R⁷³ G⁴⁰ 3425 R⁷⁴ G³⁷ 3426 R⁷⁴ G³⁸ 3427 R⁷⁴ G³⁹ 3428 R⁷⁴ G⁴⁰ 3429 R⁷⁵ G³⁷ 3430 R⁷⁵ G³⁸ 3431 R⁷⁵ G³⁹ 3432 R⁷⁵ G⁴⁰ 3433 R⁷⁶ G³⁷ 3434 R⁷⁶ G³⁸ 3435 R⁷⁶ G³⁹ 3436 R⁷⁶ G⁴⁰ 3437 R⁷⁷ G³⁷ 3438 R⁷⁷ G³⁸ 3439 R⁷⁷ G³⁹ 3440 R⁷⁷ G⁴⁰ 3441 R⁷⁸ G³⁷ 3442 R⁷⁸ G³⁸ 3443 R⁷⁸ G³⁹ 3444 R⁷⁸ G⁴⁰ 3445 R⁷⁹ G³⁷ 3446 R⁷⁹ G³⁸ 3447 R⁷⁹ G³⁹ 3448 R⁷⁹ G⁴⁰ 3449 R⁸⁰ G³⁷ 3450 R⁸⁰ G³⁸ 3451 R⁸⁰ G³⁹ 3452 R⁸⁰ G⁴⁰ 3453 R⁸¹ G³⁷ 3454 R⁸¹ G³⁸ 3455 R⁸¹ G³⁹ 3456 R⁸¹ G⁴⁰ 3457 R⁸² G³⁷ 3458 R⁸² G³⁸ 3459 R⁸² G³⁹ 3460 R⁸² G⁴⁰ 3461 R⁸³ G³⁷ 3462 R⁸³ G³⁸ 3463 R⁸³ G³⁹ 3464 R⁸³ G⁴⁰ 3465 R⁸⁴ G³⁷ 3466 R⁸⁴ G³⁸ 3467 R⁸⁴ G³⁹ 3468 R⁸⁴ G⁴⁰ 3469 R⁸⁵ G³⁷ 3470 R⁸⁵ G³⁸ 3471 R⁸⁵ G³⁹ 3472 R⁸⁵ G⁴⁰ 3473 R⁸⁶ G³⁷ 3474 R⁸⁶ G³⁸ 3475 R⁸⁶ G³⁹ 3476 R⁸⁶ G⁴⁰ 3477 R⁸⁷ G³⁷ 3478 R⁸⁷ G³⁸ 3479 R⁸⁷ G³⁹ 3480 R⁸⁷ G⁴⁰ 3481 R¹ G⁴¹ 3482 R¹ G⁴² 3483 R¹ G⁴³ 3484 R¹ G⁴⁴ 3485 R² G⁴¹ 3486 R² G⁴² 3487 R² G⁴³ 3488 R² G⁴⁴ 3489 R³ G⁴¹ 3490 R³ G⁴² 3491 R³ G⁴³ 3492 R³ G⁴⁴ 3493 R⁴ G⁴¹ 3494 R⁴ G⁴² 3495 R⁴ G⁴³ 3496 R⁴ G⁴⁴ 3497 R⁵ G⁴¹ 3498 R⁵ G⁴² 3499 R⁵ G⁴³ 3500 R⁵ G⁴⁴ 3501 R⁶ G⁴¹ 3502 R⁶ G⁴² 3503 R⁶ G⁴³ 3504 R⁶ G⁴⁴ 3505 R⁷ G⁴¹ 3506 R⁷ G⁴² 3507 R⁷ G⁴³ 3508 R⁷ G⁴⁴ 3509 R⁸ G⁴¹ 3510 R⁸ G⁴² 3511 R⁸ G⁴³ 3512 R⁸ G⁴⁴ 3513 R⁹ G⁴¹ 3514 R⁹ G⁴² 3515 R⁹ G⁴³ 3516 R⁹ G⁴⁴ 3517 R¹⁰ G⁴¹ 3518 R¹⁰ G⁴² 3519 R¹⁰ G⁴³ 3520 R¹⁰ G⁴⁴ 3521 R¹¹ G⁴¹ 3522 R¹¹ G⁴² 3523 R¹¹ G⁴³ 3524 R¹¹ G⁴⁴ 3525 R¹² G⁴¹ 3526 R¹² G⁴² 3527 R¹² G⁴³ 3528 R¹² G⁴⁴ 3529 R¹³ G⁴¹ 3530 R¹³ G⁴² 3531 R¹³ G⁴³ 3532 R¹³ G⁴⁴ 3533 R¹⁴ G⁴¹ 3534 R¹⁴ G⁴² 3535 R¹⁴ G⁴³ 3536 R¹⁴ G⁴⁴ 3537 R¹⁵ G⁴¹ 3538 R¹⁵ G⁴² 3539 R¹⁵ G⁴³ 3540 R¹⁵ G⁴⁴ 3541 R¹⁶ G⁴¹ 3542 R¹⁶ G⁴² 3543 R¹⁶ G⁴³ 3544 R¹⁶ G⁴⁴ 3545 R¹⁷ G⁴¹ 3546 R¹⁷ G⁴² 3547 R¹⁷ G⁴³ 3548 R¹⁷ G⁴⁴ 3549 R¹⁸ G⁴¹ 3550 R¹⁸ G⁴² 3551 R¹⁸ G⁴³ 3552 R¹⁸ G⁴⁴ 3553 R¹⁹ G⁴¹ 3554 R¹⁹ G⁴² 3555 R¹⁹ G⁴³ 3556 R¹⁹ G⁴⁴ 3557 R²⁰ G⁴¹ 3558 R²⁰ G⁴² 3559 R²⁰ G⁴³ 3560 R²⁰ G⁴⁴ 3561 R²¹ G⁴¹ 3562 R²¹ G⁴² 3563 R²¹ G⁴³ 3564 R²¹ G⁴⁴ 3565 R²² G⁴¹ 3566 R²² G⁴² 3567 R²² G⁴³ 3568 R²² G⁴⁴ 3569 R²³ G⁴¹ 3570 R²³ G⁴² 3571 R²³ G⁴³ 3572 R²³ G⁴⁴ 3573 R²⁴ G⁴¹ 3574 R²⁴ G⁴² 3575 R²⁴ G⁴³ 3576 R²⁴ G⁴⁴ 3577 R²⁵ G⁴¹ 3578 R²⁵ G⁴² 3579 R²⁵ G⁴³ 3580 R²⁵ G⁴⁴ 3581 R²⁶ G⁴¹ 3582 R²⁶ G⁴² 3583 R²⁶ G⁴³ 3584 R²⁶ G⁴⁴ 3585 R²⁷ G⁴¹ 3586 R²⁷ G⁴² 3587 R²⁷ G⁴³ 3588 R²⁷ G⁴⁴ 3589 R²⁸ G⁴¹ 3590 R²⁸ G⁴² 3591 R²⁸ G⁴³ 3592 R²⁸ G⁴⁴ 3593 R²⁹ G⁴¹ 3594 R²⁹ G⁴² 3595 R²⁹ G⁴³ 3596 R²⁹ G⁴⁴ 3597 R³⁰ G⁴¹ 3598 R³⁰ G⁴² 3599 R³⁰ G⁴³ 3600 R³⁰ G⁴⁴ 3601 R³¹ G⁴¹ 3602 R³¹ G⁴² 3603 R³¹ G⁴³ 3604 R³¹ G⁴⁴ 3605 R³² G⁴¹ 3606 R³² G⁴² 3607 R³² G⁴³ 3608 R³² G⁴⁴ 3609 R³³ G⁴¹ 3610 R³³ G⁴² 3611 R³³ G⁴³ 3612 R³³ G⁴⁴ 3613 R³⁴ G⁴¹ 3614 R³⁴ G⁴² 3615 R³⁴ G⁴³ 3616 R³⁴ G⁴⁴ 3617 R³⁵ G⁴¹ 3618 R³⁵ G⁴² 3619 R³⁵ G⁴³ 3620 R³⁵ G⁴⁴ 3621 R³⁶ G⁴¹ 3622 R³⁶ G⁴² 3623 R³⁶ G⁴³ 3624 R³⁶ G⁴⁴ 3625 R³⁷ G⁴¹ 3626 R³⁷ G⁴² 3627 R³⁷ G⁴³ 3628 R³⁷ G⁴⁴ 3629 R³⁸ G⁴¹ 3630 R³⁸ G⁴² 3631 R³⁸ G⁴³ 3632 R³⁸ G⁴⁴ 3633 R³⁹ G⁴¹ 3634 R³⁹ G⁴² 3635 R³⁹ G⁴³ 3636 R³⁹ G⁴⁴ 3637 R⁴⁰ G⁴¹ 3638 R⁴⁰ G⁴² 3639 R⁴⁰ G⁴³ 3640 R⁴⁰ G⁴⁴ 3641 R⁴¹ G⁴¹ 3642 R⁴¹ G⁴² 3643 R⁴¹ G⁴³ 3644 R⁴¹ G⁴⁴ 3645 R⁴² G⁴¹ 3646 R⁴² G⁴² 3647 R⁴² G⁴³ 3648 R⁴² G⁴⁴ 3649 R⁴³ G⁴¹ 3650 R⁴³ G⁴² 3651 R⁴³ G⁴³ 3652 R⁴³ G⁴⁴ 3653 R⁴⁴ G⁴¹ 3654 R⁴⁴ G⁴² 3655 R⁴⁴ G⁴³ 3656 R⁴⁴ G⁴⁴ 3657 R⁴⁵ G⁴¹ 3658 R⁴⁵ G⁴² 3659 R⁴⁵ G⁴³ 3660 R⁴⁵ G⁴⁴ 3661 R⁴⁶ G⁴¹ 3662 R⁴⁶ G⁴² 3663 R⁴⁶ G⁴³ 3664 R⁴⁶ G⁴⁴ 3665 R⁴⁷ G⁴¹ 3666 R⁴⁷ G⁴² 3667 R⁴⁷ G⁴³ 3668 R⁴⁷ G⁴⁴ 3669 R⁴⁸ G⁴¹ 3670 R⁴⁸ G⁴² 3671 R⁴⁸ G⁴³ 3672 R⁴⁸ G⁴⁴ 3673 R⁴⁹ G⁴¹ 3674 R⁴⁹ G⁴² 3675 R⁴⁹ G⁴³ 3676 R⁴⁹ G⁴⁴ 3677 R⁵⁰ G⁴¹ 3678 R⁵⁰ G⁴² 3679 R⁵⁰ G⁴³ 3680 R⁵⁰ G⁴⁴ 3681 R⁵¹ G⁴¹ 3682 R⁵¹ G⁴² 3683 R⁵¹ G⁴³ 3684 R⁵¹ G⁴⁴ 3685 R⁵² G⁴¹ 3686 R⁵² G⁴² 3687 R⁵² G⁴³ 3688 R⁵² G⁴⁴ 3689 R⁵³ G⁴¹ 3690 R⁵³ G⁴² 3691 R⁵³ G⁴³ 3692 R⁵³ G⁴⁴ 3693 R⁵⁴ G⁴¹ 3694 R⁵⁴ G⁴² 3695 R⁵⁴ G⁴³ 3696 R⁵⁴ G⁴⁴ 3697 R⁵⁵ G⁴¹ 3698 R⁵⁵ G⁴² 3699 R⁵⁵ G⁴³ 3700 R⁵⁵ G⁴⁴ 3701 R⁵⁶ G⁴¹ 3702 R⁵⁶ G⁴² 3703 R⁵⁶ G⁴³ 3704 R⁵⁶ G⁴⁴ 3705 R⁵⁷ G⁴¹ 3706 R⁵⁷ G⁴² 3707 R⁵⁷ G⁴³ 3708 R⁵⁷ G⁴⁴ 3709 R⁵⁸ G⁴¹ 3710 R⁵⁸ G⁴² 3711 R⁵⁸ G⁴³ 3712 R⁵⁸ G⁴⁴ 3713 R⁵⁹ G⁴¹ 3714 R⁵⁹ G⁴² 3715 R⁵⁹ G⁴³ 3716 R⁵⁹ G⁴⁴ 3717 R⁶⁰ G⁴¹ 3718 R⁶⁰ G⁴² 3719 R⁶⁰ G⁴³ 3720 R⁶⁰ G⁴⁴ 3721 R⁶¹ G⁴¹ 3722 R⁶¹ G⁴² 3723 R⁶¹ G⁴³ 3724 R⁶¹ G⁴⁴ 3725 R⁶² G⁴¹ 3726 R⁶² G⁴² 3727 R⁶² G⁴³ 3728 R⁶² G⁴⁴ 3729 R⁶³ G⁴¹ 3730 R⁶³ G⁴² 3731 R⁶³ G⁴³ 3732 R⁶³ G⁴⁴ 3733 R⁶⁴ G⁴¹ 3734 R⁶⁴ G⁴² 3735 R⁶⁴ G⁴³ 3736 R⁶⁴ G⁴⁴ 3737 R⁶⁵ G⁴¹ 3738 R⁶⁵ G⁴² 3739 R⁶⁵ G⁴³ 3740 R⁶⁵ G⁴⁴ 3741 R⁶⁶ G⁴¹ 3742 R⁶⁶ G⁴² 3743 R⁶⁶ G⁴³ 3744 R⁶⁶ G⁴⁴ 3745 R⁶⁷ G⁴¹ 3746 R⁶⁷ G⁴² 3747 R⁶⁷ G⁴³ 3748 R⁶⁷ G⁴⁴ 3749 R⁶⁸ G⁴¹ 3750 R⁶⁸ G⁴² 3751 R⁶⁸ G⁴³ 3752 R⁶⁸ G⁴⁴ 3753 R⁶⁹ G⁴¹ 3754 R⁶⁹ G⁴² 3755 R⁶⁹ G⁴³ 3756 R⁶⁹ G⁴⁴ 3757 R⁷⁰ G⁴¹ 3758 R⁷⁰ G⁴² 3759 R⁷⁰ G⁴³ 3760 R⁷⁰ G⁴⁴ 3761 R⁷¹ G⁴¹ 3762 R⁷¹ G⁴² 3763 R⁷¹ G⁴³ 3764 R⁷¹ G⁴⁴ 3765 R⁷² G⁴¹ 3766 R⁷² G⁴² 3767 R⁷² G⁴³ 3768 R⁷² G⁴⁴ 3769 R⁷³ G⁴¹ 3770 R⁷³ G⁴² 3771 R⁷³ G⁴³ 3772 R⁷³ G⁴⁴ 3773 R⁷⁴ G⁴¹ 3774 R⁷⁴ G⁴² 3775 R⁷⁴ G⁴³ 3776 R⁷⁴ G⁴⁴ 3777 R⁷⁵ G⁴¹ 3778 R⁷⁵ G⁴² 3779 R⁷⁵ G⁴³ 3780 R⁷⁵ G⁴⁴ 3781 R⁷⁶ G⁴¹ 3782 R⁷⁶ G⁴² 3783 R⁷⁶ G⁴³ 3784 R⁷⁶ G⁴⁴ 3785 R⁷⁷ G⁴¹ 3786 R⁷⁷ G⁴² 3787 R⁷⁷ G⁴³ 3788 R⁷⁷ G⁴⁴ 3789 R⁷⁸ G⁴¹ 3790 R⁷⁸ G⁴² 3791 R⁷⁸ G⁴³ 3792 R⁷⁸ G⁴⁴ 3793 R⁷⁹ G⁴¹ 3794 R⁷⁹ G⁴² 3795 R⁷⁹ G⁴³ 3796 R⁷⁹ G⁴⁴ 3797 R⁸⁰ G⁴¹ 3798 R⁸⁰ G⁴² 3799 R⁸⁰ G⁴³ 3800 R⁸⁰ G⁴⁴ 3801 R⁸¹ G⁴¹ 3802 R⁸¹ G⁴² 3803 R⁸¹ G⁴³ 3804 R⁸¹ G⁴⁴ 3805 R⁸² G⁴¹ 3806 R⁸² G⁴² 3807 R⁸² G⁴³ 3808 R⁸² G⁴⁴ 3809 R⁸³ G⁴¹ 3810 R⁸³ G⁴² 3811 R⁸³ G⁴³ 3812 R⁸³ G⁴⁴ 3813 R⁸⁴ G⁴¹ 3814 R⁸⁴ G⁴² 3815 R⁸⁴ G⁴³ 3816 R⁸⁴ G⁴⁴ 3817 R⁸⁵ G⁴¹ 3818 R⁸⁵ G⁴² 3819 R⁸⁵ G⁴³ 3820 R⁸⁵ G⁴⁴ 3821 R⁸⁶ G⁴¹ 3822 R⁸⁶ G⁴² 3823 R⁸⁶ G⁴³ 3824 R⁸⁶ G⁴⁴ 3825 R⁸⁷ G⁴¹ 3826 R⁸⁷ G⁴² 3827 R⁸⁷ G⁴³ 3828 R⁸⁷ G⁴⁴ 3829 R¹ G⁴⁵ 3830 R¹ G⁴⁶ 3831 R¹ G⁴⁷ 3832 R¹ G⁴⁸ 3833 R² G⁴⁵ 3834 R² G⁴⁶ 3835 R² G⁴⁷ 3836 R² G⁴⁸ 3837 R³ G⁴⁵ 3838 R³ G⁴⁶ 3839 R³ G⁴⁷ 3840 R³ G⁴⁸ 3841 R⁴ G⁴⁵ 3842 R⁴ G⁴⁶ 3843 R⁴ G⁴⁷ 3844 R⁴ G⁴⁸ 3845 R⁵ G⁴⁵ 3846 R⁵ G⁴⁶ 3847 R⁵ G⁴⁷ 3848 R⁵ G⁴⁸ 3849 R⁶ G⁴⁵ 3850 R⁶ G⁴⁶ 3851 R⁶ G⁴⁷ 3852 R⁶ G⁴⁸ 3853 R⁷ G⁴⁵ 3854 R⁷ G⁴⁶ 3855 R⁷ G⁴⁷ 3856 R⁷ G⁴⁸ 3857 R⁸ G⁴⁵ 3858 R⁸ G⁴⁶ 3859 R⁸ G⁴⁷ 3860 R⁸ G⁴⁸ 3861 R⁹ G⁴⁵ 3862 R⁹ G⁴⁶ 3863 R⁹ G⁴⁷ 3864 R⁹ G⁴⁸ 3865 R¹⁰ G⁴⁵ 3866 R¹⁰ G⁴⁶ 3867 R¹⁰ G⁴⁷ 3868 R¹⁰ G⁴⁸ 3869 R¹¹ G⁴⁵ 3870 R¹¹ G⁴⁶ 3871 R¹¹ G⁴⁷ 3872 R¹¹ G⁴⁸ 3873 R¹² G⁴⁵ 3874 R¹² G⁴⁶ 3875 R¹² G⁴⁷ 3876 R¹² G⁴⁸ 3877 R¹³ G⁴⁵ 3878 R¹³ G⁴⁶ 3879 R¹³ G⁴⁷ 3880 R¹³ G⁴⁸ 3881 R¹⁴ G⁴⁵ 3882 R¹⁴ G⁴⁶ 3883 R¹⁴ G⁴⁷ 3884 R¹⁴ G⁴⁸ 3885 R¹⁵ G⁴⁵ 3886 R¹⁵ G⁴⁶ 3887 R¹⁵ G⁴⁷ 3888 R¹⁵ G⁴⁸ 3889 R¹⁶ G⁴⁵ 3890 R¹⁶ G⁴⁶ 3891 R¹⁶ G⁴⁷ 3892 R¹⁶ G⁴⁸ 3893 R¹⁷ G⁴⁵ 3894 R¹⁷ G⁴⁶ 3895 R¹⁷ G⁴⁷ 3896 R¹⁷ G⁴⁸ 3897 R¹⁸ G⁴⁵ 3898 R¹⁸ G⁴⁶ 3899 R¹⁸ G⁴⁷ 3900 R¹⁸ G⁴⁸ 3901 R¹⁹ G⁴⁵ 3902 R¹⁹ G⁴⁶ 3903 R¹⁹ G⁴⁷ 3904 R¹⁹ G⁴⁸ 3905 R²⁰ G⁴⁵ 3906 R²⁰ G⁴⁶ 3907 R²⁰ G⁴⁷ 3908 R²⁰ G⁴⁸ 3909 R²¹ G⁴⁵ 3910 R²¹ G⁴⁶ 3911 R²¹ G⁴⁷ 3912 R²¹ G⁴⁸ 3913 R²² G⁴⁵ 3914 R²² G⁴⁶ 3915 R²² G⁴⁷ 3916 R²² G⁴⁸ 3917 R²³ G⁴⁵ 3918 R²³ G⁴⁶ 3919 R²³ G⁴⁷ 3920 R²³ G⁴⁸ 3921 R²⁴ G⁴⁵ 3922 R²⁴ G⁴⁶ 3923 R²⁴ G⁴⁷ 3924 R²⁴ G⁴⁸ 3925 R²⁵ G⁴⁵ 3926 R²⁵ G⁴⁶ 3927 R²⁵ G⁴⁷ 3928 R²⁵ G⁴⁸ 3929 R²⁶ G⁴⁵ 3930 R²⁶ G⁴⁶ 3931 R²⁶ G⁴⁷ 3932 R²⁶ G⁴⁸ 3933 R²⁷ G⁴⁵ 3934 R²⁷ G⁴⁶ 3935 R²⁷ G⁴⁷ 3936 R²⁷ G⁴⁸ 3937 R²⁸ G⁴⁵ 3938 R²⁸ G⁴⁶ 3939 R²⁸ G⁴⁷ 3940 R²⁸ G⁴⁸ 3941 R²⁹ G⁴⁵ 3942 R²⁹ G⁴⁶ 3943 R²⁹ G⁴⁷ 3944 R²⁹ G⁴⁸ 3945 R³⁰ G⁴⁵ 3946 R³⁰ G⁴⁶ 3947 R³⁰ G⁴⁷ 3948 R³⁰ G⁴⁸ 3949 R³¹ G⁴⁵ 3950 R³¹ G⁴⁶ 3951 R³¹ G⁴⁷ 3952 R³¹ G⁴⁸ 3953 R³² G⁴⁵ 3954 R³² G⁴⁶ 3955 R³² G⁴⁷ 3956 R³² G⁴⁸ 3957 R³³ G⁴⁵ 3958 R³³ G⁴⁶ 3959 R³³ G⁴⁷ 3960 R³³ G⁴⁸ 3961 R³⁴ G⁴⁵ 3962 R³⁴ G⁴⁶ 3963 R³⁴ G⁴⁷ 3964 R³⁴ G⁴⁸ 3965 R³⁵ G⁴⁵ 3966 R³⁵ G⁴⁶ 3967 R³⁵ G⁴⁷ 3968 R³⁵ G⁴⁸ 3969 R³⁶ G⁴⁵ 3970 R³⁶ G⁴⁶ 3971 R³⁶ G⁴⁷ 3972 R³⁶ G⁴⁸ 3973 R³⁷ G⁴⁵ 3974 R³⁷ G⁴⁶ 3975 R³⁷ G⁴⁷ 3976 R³⁷ G⁴⁸ 3977 R³⁸ G⁴⁵ 3978 R³⁸ G⁴⁶ 3979 R³⁸ G⁴⁷ 3980 R³⁸ G⁴⁸ 3981 R³⁹ G⁴⁵ 3982 R³⁹ G⁴⁶ 3983 R³⁹ G⁴⁷ 3984 R³⁹ G⁴⁸ 3985 R⁴⁰ G⁴⁵ 3986 R⁴⁰ G⁴⁶ 3987 R⁴⁰ G⁴⁷ 3988 R⁴⁰ G⁴⁸ 3989 R⁴¹ G⁴⁵ 3990 R⁴¹ G⁴⁶ 3991 R⁴¹ G⁴⁷ 3992 R⁴¹ G⁴⁸ 3993 R⁴² G⁴⁵ 3994 R⁴² G⁴⁶ 3995 R⁴² G⁴⁷ 3996 R⁴² G⁴⁸ 3997 R⁴³ G⁴⁵ 3998 R⁴³ G⁴⁶ 3999 R⁴³ G⁴⁷ 4000 R⁴³ G⁴⁸ 4001 R⁴⁴ G⁴⁵ 4002 R⁴⁴ G⁴⁶ 4003 R⁴⁴ G⁴⁷ 4004 R⁴⁴ G⁴⁸ 4005 R⁴⁵ G⁴⁵ 4006 R⁴⁵ G⁴⁶ 4007 R⁴⁵ G⁴⁷ 4008 R⁴⁵ G⁴⁸ 4009 R⁴⁶ G⁴⁵ 4010 R⁴⁶ G⁴⁶ 4011 R⁴⁶ G⁴⁷ 4012 R⁴⁶ G⁴⁸ 4013 R⁴⁷ G⁴⁵ 4014 R⁴⁷ G⁴⁶ 4015 R⁴⁷ G⁴⁷ 4016 R⁴⁷ G⁴⁸ 4017 R⁴⁸ G⁴⁵ 4018 R⁴⁸ G⁴⁶ 4019 R⁴⁸ G⁴⁷ 4020 R⁴⁸ G⁴⁸ 4021 R⁴⁹ G⁴⁵ 4022 R⁴⁹ G⁴⁶ 4023 R⁴⁹ G⁴⁷ 4024 R⁴⁹ G⁴⁸ 4025 R⁵⁰ G⁴⁵ 4026 R⁵⁰ G⁴⁶ 4027 R⁵⁰ G⁴⁷ 4028 R⁵⁰ G⁴⁸ 4029 R⁵¹ G⁴⁵ 4030 R⁵¹ G⁴⁶ 4031 R⁵¹ G⁴⁷ 4032 R⁵¹ G⁴⁸ 4033 R⁵² G⁴⁵ 4034 R⁵² G⁴⁶ 4035 R⁵² G⁴⁷ 4036 R⁵² G⁴⁸ 4037 R⁵³ G⁴⁵ 4038 R⁵³ G⁴⁶ 4039 R⁵³ G⁴⁷ 4040 R⁵³ G⁴⁸ 4041 R⁵⁴ G⁴⁵ 4042 R⁵⁴ G⁴⁶ 4043 R⁵⁴ G⁴⁷ 4044 R⁵⁴ G⁴⁸ 4045 R⁵⁵ G⁴⁵ 4046 R⁵⁵ G⁴⁶ 4047 R⁵⁵ G⁴⁷ 4048 R⁵⁵ G⁴⁸ 4049 R⁵⁶ G⁴⁵ 4050 R⁵⁶ G⁴⁶ 4051 R⁵⁶ G⁴⁷ 4052 R⁵⁶ G⁴⁸ 4053 R⁵⁷ G⁴⁵ 4054 R⁵⁷ G⁴⁶ 4055 R⁵⁷ G⁴⁷ 4056 R⁵⁷ G⁴⁸ 4057 R⁵⁸ G⁴⁵ 4058 R⁵⁸ G⁴⁶ 4059 R⁵⁸ G⁴⁷ 4060 R⁵⁸ G⁴⁸ 4061 R⁵⁹ G⁴⁵ 4062 R⁵⁹ G⁴⁶ 4063 R⁵⁹ G⁴⁷ 4064 R⁵⁹ G⁴⁸ 4065 R⁶⁰ G⁴⁵ 4066 R⁶⁰ G⁴⁶ 4067 R⁶⁰ G⁴⁷ 4068 R⁶⁰ G⁴⁸ 4069 R⁶¹ G⁴⁵ 4070 R⁶¹ G⁴⁶ 4071 R⁶¹ G⁴⁷ 4072 R⁶¹ G⁴⁸ 4073 R⁶² G⁴⁵ 4074 R⁶² G⁴⁶ 4075 R⁶² G⁴⁷ 4076 R⁶² G⁴⁸ 4077 R⁶³ G⁴⁵ 4078 R⁶³ G⁴⁶ 4079 R⁶³ G⁴⁷ 4080 R⁶³ G⁴⁸ 4081 R⁶⁴ G⁴⁵ 4082 R⁶⁴ G⁴⁶ 4083 R⁶⁴ G⁴⁷ 4084 R⁶⁴ G⁴⁸ 4085 R⁶⁵ G⁴⁵ 4086 R⁶⁵ G⁴⁶ 4087 R⁶⁵ G⁴⁷ 4088 R⁶⁵ G⁴⁸ 4089 R⁶⁶ G⁴⁵ 4090 R⁶⁶ G⁴⁶ 4091 R⁶⁶ G⁴⁷ 4092 R⁶⁶ G⁴⁸ 4093 R⁶⁷ G⁴⁵ 4094 R⁶⁷ G⁴⁶ 4095 R⁶⁷ G⁴⁷ 4096 R⁶⁷ G⁴⁸ 4097 R⁶⁸ G⁴⁵ 4098 R⁶⁸ G⁴⁶ 4099 R⁶⁸ G⁴⁷ 4100 R⁶⁸ G⁴⁸ 4101 R⁶⁹ G⁴⁵ 4102 R⁶⁹ G⁴⁶ 4103 R⁶⁹ G⁴⁷ 4104 R⁶⁹ G⁴⁸ 4105 R⁷⁰ G⁴⁵ 4106 R⁷⁰ G⁴⁶ 4107 R⁷⁰ G⁴⁷ 4108 R⁷⁰ G⁴⁸ 4109 R⁷¹ G⁴⁵ 4110 R⁷¹ G⁴⁶ 4111 R⁷¹ G⁴⁷ 4112 R⁷¹ G⁴⁸ 4113 R⁷² G⁴⁵ 4114 R⁷² G⁴⁶ 4115 R⁷² G⁴⁷ 4116 R⁷² G⁴⁸ 4117 R⁷³ G⁴⁵ 4118 R⁷³ G⁴⁶ 4119 R⁷³ G⁴⁷ 4120 R⁷³ G⁴⁸ 4121 R⁷⁴ G⁴⁵ 4122 R⁷⁴ G⁴⁶ 4123 R⁷⁴ G⁴⁷ 4124 R⁷⁴ G⁴⁸ 4125 R⁷⁵ G⁴⁵ 4126 R⁷⁵ G⁴⁶ 4127 R⁷⁵ G⁴⁷ 4128 R⁷⁵ G⁴⁸ 4129 R⁷⁶ G⁴⁵ 4130 R⁷⁶ G⁴⁶ 4131 R⁷⁶ G⁴⁷ 4132 R⁷⁶ G⁴⁸ 4133 R⁷⁷ G⁴⁵ 4134 R⁷⁷ G⁴⁶ 4135 R⁷⁷ G⁴⁷ 4136 R⁷⁷ G⁴⁸ 4137 R⁷⁸ G⁴⁵ 4138 R⁷⁸ G⁴⁶ 4139 R⁷⁸ G⁴⁷ 4140 R⁷⁸ G⁴⁸ 4141 R⁷⁹ G⁴⁵ 4142 R⁷⁹ G⁴⁶ 4143 R⁷⁹ G⁴⁷ 4144 R⁷⁹ G⁴⁸ 4145 R⁸⁰ G⁴⁵ 4146 R⁸⁰ G⁴⁶ 4147 R⁸⁰ G⁴⁷ 4148 R⁸⁰ G⁴⁸ 4149 R⁸¹ G⁴⁵ 4150 R⁸¹ G⁴⁶ 4151 R⁸¹ G⁴⁷ 4152 R⁸¹ G⁴⁸ 4153 R⁸² G⁴⁵ 4154 R⁸² G⁴⁶ 4155 R⁸² G⁴⁷ 4156 R⁸² G⁴⁸ 4157 R⁸³ G⁴⁵ 4158 R⁸³ G⁴⁶ 4159 R⁸³ G⁴⁷ 4160 R⁸³ G⁴⁸ 4161 R⁸⁴ G⁴⁵ 4162 R⁸⁴ G⁴⁶ 4163 R⁸⁴ G⁴⁷ 4164 R⁸⁴ G⁴⁸ 4165 R⁸⁵ G⁴⁵ 4166 R⁸⁵ G⁴⁶ 4167 R⁸⁵ G⁴⁷ 4168 R⁸⁵ G⁴⁸ 4169 R⁸⁶ G⁴⁵ 4170 R⁸⁶ G⁴⁶ 4171 R⁸⁶ G⁴⁷ 4172 R⁸⁶ G⁴⁸ 4173 R⁸⁷ G⁴⁵ 4174 R⁸⁷ G⁴⁶ 4175 R⁸⁷ G⁴⁷ 4176 R⁸⁷ G⁴⁸ 4177 R¹ G⁴⁹ 4178 R¹ G⁵⁰ 4179 R¹ G⁵¹ 4180 R¹ G⁵² 4181 R² G⁴⁹ 4182 R² G⁵⁰ 4183 R² G⁵¹ 4184 R² G⁵² 4185 R³ G⁴⁹ 4186 R³ G⁵⁰ 4187 R³ G⁵¹ 4188 R³ G⁵² 4189 R⁴ G⁴⁹ 4190 R⁴ G⁵⁰ 4191 R⁴ G⁵¹ 4192 R⁴ G⁵² 4193 R⁵ G⁴⁹ 4194 R⁵ G⁵⁰ 4195 R⁵ G⁵¹ 4196 R⁵ G⁵² 4197 R⁶ G⁴⁹ 4198 R⁶ G⁵⁰ 4199 R⁶ G⁵¹ 4200 R⁶ G⁵² 4201 R⁷ G⁴⁹ 4202 R⁷ G⁵⁰ 4203 R⁷ G⁵¹ 4204 R⁷ G⁵² 4205 R⁸ G⁴⁹ 4206 R⁸ G⁵⁰ 4207 R⁸ G⁵¹ 4208 R⁸ G⁵² 4209 R⁹ G⁴⁹ 4210 R⁹ G⁵⁰ 4211 R⁹ G⁵¹ 4212 R⁹ G⁵² 4213 R¹⁰ G⁴⁹ 4214 R¹⁰ G⁵⁰ 4215 R¹⁰ G⁵¹ 4216 R¹⁰ G⁵² 4217 R¹¹ G⁴⁹ 4218 R¹¹ G⁵⁰ 4219 R¹¹ G⁵¹ 4220 R¹¹ G⁵² 4221 R¹² G⁴⁹ 4222 R¹² G⁵⁰ 4223 R¹² G⁵¹ 4224 R¹² G⁵² 4225 R¹³ G⁴⁹ 4226 R¹³ G⁵⁰ 4227 R¹³ G⁵¹ 4228 R¹³ G⁵² 4229 R¹⁴ G⁴⁹ 4230 R¹⁴ G⁵⁰ 4231 R¹⁴ G⁵¹ 4232 R¹⁴ G⁵² 4233 R¹⁵ G⁴⁹ 4234 R¹⁵ G⁵⁰ 4235 R¹⁵ G⁵¹ 4236 R¹⁵ G⁵² 4237 R¹⁶ G⁴⁹ 4238 R¹⁶ G⁵⁰ 4239 R¹⁶ G⁵¹ 4240 R¹⁶ G⁵² 4241 R¹⁷ G⁴⁹ 4242 R¹⁷ G⁵⁰ 4243 R¹⁷ G⁵¹ 4244 R¹⁷ G⁵² 4245 R¹⁸ G⁴⁹ 4246 R¹⁸ G⁵⁰ 4247 R¹⁸ G⁵¹ 4248 R¹⁸ G⁵² 4249 R¹⁹ G⁴⁹ 4250 R¹⁹ G⁵⁰ 4251 R¹⁹ G⁵¹ 4252 R¹⁹ G⁵² 4253 R²⁰ G⁴⁹ 4254 R²⁰ G⁵⁰ 4255 R²⁰ G⁵¹ 4256 R²⁰ G⁵² 4257 R²¹ G⁴⁹ 4258 R²¹ G⁵⁰ 4259 R²¹ G⁵¹ 4260 R²¹ G⁵² 4261 R²² G⁴⁹ 4262 R²² G⁵⁰ 4263 R²² G⁵¹ 4264 R²² G⁵² 4265 R²³ G⁴⁹ 4266 R²³ G⁵⁰ 4267 R²³ G⁵¹ 4268 R²³ G⁵² 4269 R²⁴ G⁴⁹ 4270 R²⁴ G⁵⁰ 4271 R²⁴ G⁵¹ 4272 R²⁴ G⁵² 4273 R²⁵ G⁴⁹ 4274 R²⁵ G⁵⁰ 4275 R²⁵ G⁵¹ 4276 R²⁵ G⁵² 4277 R²⁶ G⁴⁹ 4278 R²⁶ G⁵⁰ 4279 R²⁶ G⁵¹ 4280 R²⁶ G⁵² 4281 R²⁷ G⁴⁹ 4282 R²⁷ G⁵⁰ 4283 R²⁷ G⁵¹ 4284 R²⁷ G⁵² 4285 R²⁸ G⁴⁹ 4286 R²⁸ G⁵⁰ 4287 R²⁸ G⁵¹ 4288 R²⁸ G⁵² 4289 R²⁹ G⁴⁹ 4290 R²⁹ G⁵⁰ 4291 R²⁹ G⁵¹ 4292 R²⁹ G⁵² 4293 R³⁰ G⁴⁹ 4294 R³⁰ G⁵⁰ 4295 R³⁰ G⁵¹ 4296 R³⁰ G⁵² 4297 R³¹ G⁴⁹ 4298 R³¹ G⁵⁰ 4299 R³¹ G⁵¹ 4300 R³¹ G⁵² 4301 R³² G⁴⁹ 4302 R³² G⁵⁰ 4303 R³² G⁵¹ 4304 R³² G⁵² 4305 R³³ G⁴⁹ 4306 R³³ G⁵⁰ 4307 R³³ G⁵¹ 4308 R³³ G⁵² 4309 R³⁴ G⁴⁹ 4310 R³⁴ G⁵⁰ 4311 R³⁴ G⁵¹ 4312 R³⁴ G⁵² 4313 R³⁵ G⁴⁹ 4314 R³⁵ G⁵⁰ 4315 R³⁵ G⁵¹ 4316 R³⁵ G⁵² 4317 R³⁶ G⁴⁹ 4318 R³⁶ G⁵⁰ 4319 R³⁶ G⁵¹ 4320 R³⁶ G⁵² 4321 R³⁷ G⁴⁹ 4322 R³⁷ G⁵⁰ 4323 R³⁷ G⁵¹ 4324 R³⁷ G⁵² 4325 R³⁸ G⁴⁹ 4326 R³⁸ G⁵⁰ 4327 R³⁸ G⁵¹ 4328 R³⁸ G⁵² 4329 R³⁹ G⁴⁹ 4330 R³⁹ G⁵⁰ 4331 R³⁹ G⁵¹ 4332 R³⁹ G⁵² 4333 R⁴⁰ G⁴⁹ 4334 R⁴⁰ G⁵⁰ 4335 R⁴⁰ G⁵¹ 4336 R⁴⁰ G⁵² 4337 R⁴¹ G⁴⁹ 4338 R⁴¹ G⁵⁰ 4339 R⁴¹ G⁵¹ 4340 R⁴¹ G⁵² 4341 R⁴² G⁴⁹ 4342 R⁴² G⁵⁰ 4343 R⁴² G⁵¹ 4344 R⁴² G⁵² 4345 R⁴³ G⁴⁹ 4346 R⁴³ G⁵⁰ 4347 R⁴³ G⁵¹ 4348 R⁴³ G⁵² 4349 R⁴⁴ G⁴⁹ 4350 R⁴⁴ G⁵⁰ 4351 R⁴⁴ G⁵¹ 4352 R⁴⁴ G⁵² 4353 R⁴⁵ G⁴⁹ 4354 R⁴⁵ G⁵⁰ 4355 R⁴⁵ G⁵¹ 4356 R⁴⁵ G⁵² 4357 R⁴⁶ G⁴⁹ 4358 R⁴⁶ G⁵⁰ 4359 R⁴⁶ G⁵¹ 4360 R⁴⁶ G⁵² 4361 R⁴⁷ G⁴⁹ 4362 R⁴⁷ G⁵⁰ 4363 R⁴⁷ G⁵¹ 4364 R⁴⁷ G⁵² 4365 R⁴⁸ G⁴⁹ 4366 R⁴⁸ G⁵⁰ 4367 R⁴⁸ G⁵¹ 4368 R⁴⁸ G⁵² 4369 R⁴⁹ G⁴⁹ 4370 R⁴⁹ G⁵⁰ 4371 R⁴⁹ G⁵¹ 4372 R⁴⁹ G⁵² 4373 R⁵⁰ G⁴⁹ 4374 R⁵⁰ G⁵⁰ 4375 R⁵⁰ G⁵¹ 4376 R⁵⁰ G⁵² 4377 R⁵¹ G⁴⁹ 4378 R⁵¹ G⁵⁰ 4379 R⁵¹ G⁵¹ 4380 R⁵¹ G⁵² 4381 R⁵² G⁴⁹ 4382 R⁵² G⁵⁰ 4383 R⁵² G⁵¹ 4384 R⁵² G⁵² 4385 R⁵³ G⁴⁹ 4386 R⁵³ G⁵⁰ 4387 R⁵³ G⁵¹ 4388 R⁵³ G⁵² 4389 R⁵⁴ G⁴⁹ 4390 R⁵⁴ G⁵⁰ 4391 R⁵⁴ G⁵¹ 4392 R⁵⁴ G⁵² 4393 R⁵⁵ G⁴⁹ 4394 R⁵⁵ G⁵⁰ 4395 R⁵⁵ G⁵¹ 4396 R⁵⁵ G⁵² 4397 R⁵⁶ G⁴⁹ 4398 R⁵⁶ G⁵⁰ 4399 R⁵⁶ G⁵¹ 4400 R⁵⁶ G⁵² 4401 R⁵⁷ G⁴⁹ 4402 R⁵⁷ G⁵⁰ 4403 R⁵⁷ G⁵¹ 4404 R⁵⁷ G⁵² 4405 R⁵⁸ G⁴⁹ 4406 R⁵⁸ G⁵⁰ 4407 R⁵⁸ G⁵¹ 4408 R⁵⁸ G⁵² 4409 R⁵⁹ G⁴⁹ 4410 R⁵⁹ G⁵⁰ 4411 R⁵⁹ G⁵¹ 4412 R⁵⁹ G⁵² 4413 R⁶⁰ G⁴⁹ 4414 R⁶⁰ G⁵⁰ 4415 R⁶⁰ G⁵¹ 4416 R⁶⁰ G⁵² 4417 R⁶¹ G⁴⁹ 4418 R⁶¹ G⁵⁰ 4419 R⁶¹ G⁵¹ 4420 R⁶¹ G⁵² 4421 R⁶² G⁴⁹ 4422 R⁶² G⁵⁰ 4423 R⁶² G⁵¹ 4424 R⁶² G⁵² 4425 R⁶³ G⁴⁹ 4426 R⁶³ G⁵⁰ 4427 R⁶³ G⁵¹ 4428 R⁶³ G⁵² 4429 R⁶⁴ G⁴⁹ 4430 R⁶⁴ G⁵⁰ 4431 R⁶⁴ G⁵¹ 4432 R⁶⁴ G⁵² 4433 R⁶⁵ G⁴⁹ 4434 R⁶⁵ G⁵⁰ 4435 R⁶⁵ G⁵¹ 4436 R⁶⁵ G⁵² 4437 R⁶⁶ G⁴⁹ 4438 R⁶⁶ G⁵⁰ 4439 R⁶⁶ G⁵¹ 4440 R⁶⁶ G⁵² 4441 R⁶⁷ G⁴⁹ 4442 R⁶⁷ G⁵⁰ 4443 R⁶⁷ G⁵¹ 4444 R⁶⁷ G⁵² 4445 R⁶⁸ G⁴⁹ 4446 R⁶⁸ G⁵⁰ 4447 R⁶⁸ G⁵¹ 4448 R⁶⁸ G⁵² 4449 R⁶⁹ G⁴⁹ 4450 R⁶⁹ G⁵⁰ 4451 R⁶⁹ G⁵¹ 4452 R⁶⁹ G⁵² 4453 R⁷⁰ G⁴⁹ 4454 R⁷⁰ G⁵⁰ 4455 R⁷⁰ G⁵¹ 4456 R⁷⁰ G⁵² 4457 R⁷¹ G⁴⁹ 4458 R⁷¹ G⁵⁰ 4459 R⁷¹ G⁵¹ 4460 R⁷¹ G⁵² 4461 R⁷² G⁴⁹ 4462 R⁷² G⁵⁰ 4463 R⁷² G⁵¹ 4464 R⁷² G⁵² 4465 R⁷³ G⁴⁹ 4466 R⁷³ G⁵⁰ 4467 R⁷³ G⁵¹ 4468 R⁷³ G⁵² 4469 R⁷⁴ G⁴⁹ 4470 R⁷⁴ G⁵⁰ 4471 R⁷⁴ G⁵¹ 4472 R⁷⁴ G⁵² 4473 R⁷⁵ G⁴⁹ 4474 R⁷⁵ G⁵⁰ 4475 R⁷⁵ G⁵¹ 4476 R⁷⁵ G⁵² 4477 R⁷⁶ G⁴⁹ 4478 R⁷⁶ G⁵⁰ 4479 R⁷⁶ G⁵¹ 4480 R⁷⁶ G⁵² 4481 R⁷⁷ G⁴⁹ 4482 R⁷⁷ G⁵⁰ 4483 R⁷⁷ G⁵¹ 4484 R⁷⁷ G⁵² 4485 R⁷⁸ G⁴⁹ 4486 R⁷⁸ G⁵⁰ 4487 R⁷⁸ G⁵¹ 4488 R⁷⁸ G⁵² 4489 R⁷⁹ G⁴⁹ 4490 R⁷⁹ G⁵⁰ 4491 R⁷⁹ G⁵¹ 4492 R⁷⁹ G⁵² 4493 R⁸⁰ G⁴⁹ 4494 R⁸⁰ G⁵⁰ 4495 R⁸⁰ G⁵¹ 4496 R⁸⁰ G⁵² 4497 R⁸¹ G⁴⁹ 4498 R⁸¹ G⁵⁰ 4499 R⁸¹ G⁵¹ 4500 R⁸¹ G⁵² 4501 R⁸² G⁴⁹ 4502 R⁸² G⁵⁰ 4503 R⁸² G⁵¹ 4504 R⁸² G⁵² 4505 R⁸³ G⁴⁹ 4506 R⁸³ G⁵⁰ 4507 R⁸³ G⁵¹ 4508 R⁸³ G⁵² 4509 R⁸⁴ G⁴⁹ 4510 R⁸⁴ G⁵⁰ 4511 R⁸⁴ G⁵¹ 4512 R⁸⁴ G⁵² 4513 R⁸⁵ G⁴⁹ 4514 R⁸⁵ G⁵⁰ 4515 R⁸⁵ G⁵¹ 4516 R⁸⁵ G⁵² 4517 R⁸⁶ G⁴⁹ 4518 R⁸⁶ G⁵⁰ 4519 R⁸⁶ G⁵¹ 4520 R⁸⁶ G⁵² 4521 R⁸⁷ G⁴⁹ 4522 R⁸⁷ G⁵⁰ 4523 R⁸⁷ G⁵¹ 4524 R⁸⁷ G⁵²

where R¹ to R⁷⁸ have the structures in the following LIST 4:

and

where G¹ to G⁵² have the structures in the following LIST 5:

In some embodiments, when X in L_(Ai-m-X) is 4 it represents X in the above shown chemical structures for L_(Ai-m-X) being NH₃.

In some embodiments, the compound has a formula of M(L_(A))_(p)(L_(B))_(q)(L_(C))_(r) wherein L_(B) and L_(C) are each a bidentate ligand; and wherein p is 1, 2, or 3; q is 0, 1, or 2; r is 0, 1, or 2; and p+q+r is the oxidation state of the metal M.

In some embodiments, the compound has a formula selected from the group consisting of Ir(L_(A))₃, Ir(L_(A))(L_(B))₂, Ir(L_(A))₂(L_(B)), Ir(L_(A))₂(L_(C)), and Ir(L_(A))(L_(B))(L_(C)); and wherein L_(A), L_(B), and L_(C) are different from each other.

In some embodiments, L_(B) can be a substituted or unsubstituted phenylpyridine, and L_(C) can be a substituted or unsubstituted acetylacetonate.

In some embodiments, the compound has a formula of Pt(L_(A))(L_(B)); and wherein L_(A) and L_(B) can be same or different.

In some embodiments, L_(A) and L_(B) are connected to form a tetradentate ligand.

In some embodiments, L_(B) and L_(C) are each independently selected from the group consisting of the structures in the following LIST 6:

wherein:

T is selected from the group consisting of B, Al, Ga, and In;

each of Y¹ to Y¹³ is independently selected from the group consisting of carbon and nitrogen;

Y′ is selected from the group consisting of BR_(e), BR_(e)R_(f), NR_(e), PR_(e), P(O)R_(e), O, S, Se, C═O, C═S, C═Se, C═NR_(e), C═CR_(e)R_(f), S═O, SO₂, CR_(e)R_(f), SiR_(e)R_(f), and GeR_(e)R_(f);

R_(e) and R_(f) can be fused or joined to form a ring;

each R_(a), R_(b), R_(c), and R_(d) independently represent zero, mono, or up to a maximum allowed number of substitutions to its associated ring;

each of R_(a1), R_(b1), R_(c1), R_(d1), R_(a), R_(b), R_(c), R_(d), R_(e) and R_(f) is independently a hydrogen or a substituent selected from the group consisting of the General Substituents; and

any two adjacent R_(a), R_(b), R_(e), R_(d), R_(e) and R_(f) can be fused or joined to form a ring or form a multidentate ligand.

In some embodiments, L_(B) and L_(C) are each independently selected from the group consisting of the structures of the following LIST 7:

where:

R_(a)′, R_(b)′, and R_(c)′ each independently represent zero, mono, or up to a maximum allowed substitution to its associated ring;

each of R_(a1), R_(b1), R_(c1), R_(a), R_(b), R_(c), R_(N), R_(a)′, R_(b)′, and R_(c)′ is independently hydrogen or a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, boryl, selenyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; and

two adjacent R_(a)′, R_(b)′, and R_(c)′ can be fused or joined to form a ring or form a multidentate ligand.

In some embodiments, the compound can be selected from the group consisting of Ir(L_(A))₃, Ir(L_(A))(L_(Bk))₂, Ir(L_(A))₂(L_(Bk)), Ir(L_(A))₂(L_(Cj-I)), and Ir(L_(A))₂(L_(Cj-II)), wherein L_(A) is a ligand defined herein, each L_(Bk) is defined herein, and each of L_(Cj-I) and L_(Cj-II) is defined herein.

In some embodiments,

when the compound has formula Ir(L_(A-i-m-X))₃, i is an integer from 1 to 4524; m is an integer from 1 to 184; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₃ to Ir(L_(A4524-184-4))₃;

when the compound has formula Ir(L_(A-i-m-X))(L_(Bk))₂, i is an integer from 1 to 4524; m is an integer from 1 to 184; k is an integer from 1 to 324; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))(L_(B1))₂ to Ir(L_(A4524-184-4))(L_(B324))₂;

when the compound has formula Ir(L_(A-i-m-X))₂(L_(Bk)), i is an integer from 1 to 4524; m is an integer from 1 to 184; k is an integer from 1 to 324; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(B1)) to Ir(L_(A4524-184-4))₂(L_(B324));

when the compound has formula Ir(L_(A-i-m-X))₂(L_(Cj-I)), i is an integer from 1 to 4524; m is an integer from 1 to 184; j is an integer from 1 to 1416; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1-1))₂(L_(C1-I)) to Ir(L_(A4524-184-4))₂(L_(C1416-I)); and

when the compound has formula Ir(L_(A-i-m-X))₂(L_(Cj-II)), i is an integer from 1 to 4524; m is an integer from 1 to 184; j is an integer from 1 to 1416; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(C1-II)) to Ir(L_(A4524-184-4))₂(L_(C1416-II));

wherein when X in the formula L_(Ai-m-X) is 1, it represents the X in the chemical structure for L_(Ai-m-X) being O, when X in the formula L_(Ai-m-X) is 2, it represents the X in the chemical structure for L_(Ai-m-X) being S, when X in the formula L_(Ai-m-X) is 3, it represents the X in the chemical structure for L_(Ai-m-X) being Se, and when X in the formula L_(Ai-m-X) is 4, it represents the X in the chemical structure for L_(Ai-m-X) being NCH₃;

wherein each L_(Bk) has the structure defined in the following LIST 8:

wherein each L_(Cj-I) has a structure based on formula

and each L_(Cj-II) has a structure based on formula

wherein for each L_(Cj) in L_(Cj-I) and L_(Cj-II), R²⁰¹ and R²⁰² are each independently defined in the following LIST 9:

L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(C1) R^(D1) R^(D1) L_(C193) R^(D1) R^(D3) L_(C385) R^(D17) R^(D40) L_(C577) R^(D143) R^(D120) L_(C2) R^(D2) R^(D2) L_(C194) R^(D1) R^(D4) L_(C386) R^(D17) R^(D41) L_(C578) R^(D143) R^(D133) L_(C3) R^(D3) R^(D3) L_(C195) R^(D1) R^(D5) L_(C387) R^(D17) R^(D42) L_(C579) R^(D143) R^(D134) L_(C4) R^(D4) R^(D4) L_(C196) R^(D1) R^(D9) L_(C388) R^(D17) R^(D43) L_(C580) R^(D143) R^(D135) L_(C5) R^(D5) R^(D5) L_(C197) R^(D1) R^(D10) L_(C389) R^(D17) R^(D48) L_(C581) R^(D143) R^(D136) L_(C6) R^(D6) R^(D6) L_(C198) R^(D1) R^(D17) L_(C390) R^(D17) R^(D49) L_(C582) R^(D143) R^(D144) L_(C7) R^(D7) R^(D7) L_(C199) R^(D1) R^(D18) L_(C391) R^(D17) R^(D50) L_(C583) R^(D143) R^(D145) L_(C8) R^(D8) R^(D8) L_(C200) R^(D1) R^(D20) L_(C392) R^(D17) R^(D54) L_(C584) R^(D143) R^(D146) L_(C9) R^(D9) R^(D9) L_(C201) R^(D1) R^(D22) L_(C393) R^(D17) R^(D55) L_(C585) R^(D143) R^(D147) L_(C10) R^(D10) R^(D10) L_(C202) R^(D1) R^(D37) L_(C394) R^(D17) R^(D58) L_(C586) R^(D143) R^(D149) L_(C11) R^(D11) R^(D11) L_(C203) R^(D1) R^(D40) L_(C395) R^(D17) R^(D59) L_(C587) R^(D143) R^(D151) L_(C12) R^(D12) R^(D12) L_(C204) R^(D1) R^(D41) L_(C396) R^(D17) R^(D78) L_(C588) R^(D143) R^(D154) L_(C13) R^(D13) R^(D13) L_(C205) R^(D1) R^(D42) L_(C397) R^(D17) R^(D79) L_(C589) R^(D143) R^(D155) L_(C14) R^(D14) R^(D14) L_(C206) R^(D1) R^(D43) L_(C398) R^(D17) R^(D81) L_(C590) R^(D143) R^(D161) L_(C15) R^(D15) R^(D15) L_(C207) R^(D1) R^(D48) L_(C399) R^(D17) R^(D87) L_(C591) R^(D143) R^(D175) L_(C16) R^(D16) R^(D16) L_(C208) R^(D1) R^(D49) L_(C400) R^(D17) R^(D88) L_(C592) R^(D144) R^(D3) L_(C17) R^(D17) R^(D17) L_(C209) R^(D1) R^(D50) L_(C401) R^(D17) R^(D89) L_(C593) R^(D144) R^(D5) L_(C18) R^(D18) R^(D18) L_(C210) R^(D1) R^(D54) L_(C402) R^(D17) R^(D93) L_(C594) R^(D144) R^(D17) L_(C19) R^(D19) R^(D19) L_(C211) R^(D1) R^(D55) L_(C403) R^(D17) R^(D116) L_(C595) R^(D144) R^(D18) L_(C20) R^(D20) R^(D20) L_(C212) R^(D1) R^(D58) L_(C404) R^(D17) R^(D117) L_(C596) R^(D144) R^(D20) L_(C21) R^(D21) R^(D21) L_(C213) R^(D1) R^(D59) L_(C405) R^(D17) R^(D118) L_(C597) R^(D144) R^(D22) L_(C22) R^(D22) R^(D22) L_(C214) R^(D1) R^(D78) L_(C406) R^(D17) R^(D119) L_(C598) R^(D144) R^(D37) L_(C23) R^(D23) R^(D23) L_(C215) R^(D1) R^(D79) L_(C407) R^(D17) R^(D120) L_(C599) R^(D144) R^(D40) L_(C24) R^(D24) R^(D24) L_(C216) R^(D1) R^(D81) L_(C408) R^(D17) R^(D133) L_(C600) R^(D144) R^(D41) L_(C25) R^(D25) R^(D25) L_(C217) R^(D1) R^(D87) L_(C409) R^(D17) R^(D134) L_(C601) R^(D144) R^(D42) L_(C26) R^(D26) R^(D26) L_(C218) R^(D1) R^(D88) L_(C410) R^(D17) R^(D135) L_(C602) R^(D144) R^(D43) L_(C27) R^(D27) R^(D27) L_(C219) R^(D1) R^(D89) L_(C411) R^(D17) R^(D136) L_(C603) R^(D144) R^(D48) L_(C28) R^(D28) R^(D28) L_(C220) R^(D1) R^(D93) L_(C412) R^(D17) R^(D143) L_(C604) R^(D144) R^(D49) L_(C29) R^(D29) R^(D29) L_(C221) R^(D1) R^(D116) L_(C413) R^(D17) R^(D144) L_(C605) R^(D144) R^(D54) L_(C30) R^(D30) R^(D30) L_(C222) R^(D1) R^(D117) L_(C414) R^(D17) R^(D145) L_(C606) R^(D144) R^(D58) L_(C31) R^(D31) R^(D31) L_(C223) R^(D1) R^(D118) L_(C415) R^(D17) R^(D146) L_(C607) R^(D144) R^(D59) L_(C32) R^(D32) R^(D32) L_(C224) R^(D1) R^(D119) L_(C416) R^(D17) R^(D147) L_(C608) R^(D144) R^(D78) L_(C33) R^(D33) R^(D33) L_(C225) R^(D1) R^(D120) L_(C417) R^(D17) R^(D149) L_(C609) R^(D144) R^(D79) L_(C34) R^(D34) R^(D34) L_(C226) R^(D1) R^(D133) L_(C418) R^(D17) R^(D151) L_(C610) R^(D144) R^(D81) L_(C35) R^(D35) R^(D35) L_(C227) R^(D1) R^(D134) L_(C419) R^(D17) R^(D154) L_(C611) R^(D144) R^(D87) L_(C36) R^(D36) R^(D36) L_(C228) R^(D1) R^(D135) L_(C420) R^(D17) R^(D155) L_(C612) R^(D144) R^(D88) L_(C37) R^(D37) R^(D37) L_(C229) R^(D1) R^(D136) L_(C421) R^(D17) R^(D161) L_(C613) R^(D144) R^(D89) L_(C38) R^(D38) R^(D38) L_(C230) R^(D1) R^(D143) L_(C422) R^(D17) R^(D175) L_(C614) R^(D144) R^(D93) L_(C39) R^(D39) R^(D39) L_(C231) R^(D1) R^(D144) L_(C423) R^(D50) R^(D3) L_(C615) R^(D144) R^(D116) L_(C40) R^(D40) R^(D40) L_(C232) R^(D1) R^(D145) L_(C424) R^(D50) R^(D5) L_(C616) R^(D144) R^(D117) L_(C41) R^(D41) R^(D41) L_(C233) R^(D1) R^(D146) L_(C425) R^(D50) R^(D18) L_(C617) R^(D144) R^(D118) L_(C42) R^(D42) R^(D42) L_(C234) R^(D1) R^(D147) L_(C426) R^(D50) R^(D20) L_(C618) R^(D144) R^(D119) L_(C43) R^(D43) R^(D43) L_(C235) R^(D1) R^(D149) L_(C427) R^(D50) R^(D22) L_(C619) R^(D144) R^(D120) L_(C44) R^(D44) R^(D44) L_(C236) R^(D1) R^(D151) L_(C428) R^(D50) R^(D37) L_(C620) R^(D144) R^(D133) L_(C45) R^(D45) R^(D45) L_(C237) R^(D1) R^(D154) L_(C429) R^(D50) R^(D40) L_(C621) R^(D144) R^(D134) L_(C46) R^(D46) R^(D46) L_(C238) R^(D1) R^(D155) L_(C430) R^(D50) R^(D41) L_(C622) R^(D144) R^(D135) L_(C47) R^(D47) R^(D47) L_(C239) R^(D1) R^(D161) L_(C431) R^(D50) R^(D42) L_(C623) R^(D144) R^(D136) L_(C48) R^(D48) R^(D48) L_(C240) R^(D1) R^(D175) L_(C432) R^(D50) R^(D43) L_(C624) R^(D144) R^(D145) L_(C49) R^(D49) R^(D49) L_(C241) R^(D4) R^(D3) L_(C433) R^(D50) R^(D48) L_(C625) R^(D144) R^(D146) L_(C50) R^(D50) R^(D50) L_(C242) R^(D4) R^(D5) L_(C434) R^(D50) R^(D49) L_(C626) R^(D144) R^(D147) L_(C51) R^(D51) R^(D51) L_(C243) R^(D4) R^(D9) L_(C435) R^(D50) R^(D54) L_(C627) R^(D144) R^(D149) L_(C52) R^(D52) R^(D52) L_(C244) R^(D4) R^(D10) L_(C436) R^(D50) R^(D55) L_(C628) R^(D144) R^(D151) L_(C53) R^(D53) R^(D53) L_(C245) R^(D4) R^(D17) L_(C437) R^(D50) R^(D58) L_(C629) R^(D144) R^(D154) L_(C54) R^(D54) R^(D54) L_(C246) R^(D4) R^(D18) L_(C438) R^(D50) R^(D59) L_(C630) R^(D144) R^(D155) L_(C55) R^(D55) R^(D55) L_(C247) R^(D4) R^(D20) L_(C439) R^(D50) R^(D78) L_(C631) R^(D144) R^(D161) L_(C56) R^(D56) R^(D56) L_(C248) R^(D4) R^(D22) L_(C440) R^(D50) R^(D79) L_(C632) R^(D144) R^(D175) L_(C57) R^(D57) R^(D57) L_(C249) R^(D4) R^(D37) L_(C441) R^(D50) R^(D81) L_(C633) R^(D145) R^(D3) L_(C58) R^(D58) R^(D58) L_(C250) R^(D4) R^(D40) L_(C442) R^(D50) R^(D87) L_(C634) R^(D145) R^(D5) L_(C59) R^(D59) R^(D59) L_(C251) R^(D4) R^(D41) L_(C443) R^(D50) R^(D88) L_(C635) R^(D145) R^(D17) L_(C60) R^(D60) R^(D60) L_(C252) R^(D4) R^(D42) L_(C444) R^(D50) R^(D89) L_(C636) R^(D145) R^(D18) L_(C61) R^(D61) R^(D61) L_(C253) R^(D4) R^(D43) L_(C445) R^(D50) R^(D93) L_(C637) R^(D145) R^(D20) L_(C62) R^(D62) R^(D62) L_(C254) R^(D4) R^(D48) L_(C446) R^(D50) R^(D116) L_(C638) R^(D145) R^(D22) L_(C63) R^(D63) R^(D63) L_(C255) R^(D4) R^(D49) L_(C447) R^(D50) R^(D117) L_(C639) R^(D145) R^(D37) L_(C64) R^(D64) R^(D64) L_(C256) R^(D4) R^(D50) L_(C448) R^(D50) R^(D118) L_(C640) R^(D145) R^(D40) L_(C65) R^(D65) R^(D65) L_(C257) R^(D4) R^(D54) L_(C449) R^(D50) R^(D119) L_(C641) R^(D145) R^(D41) L_(C66) R^(D66) R^(D66) L_(C258) R^(D4) R^(D55) L_(C450) R^(D50) R^(D120) L_(C642) R^(D145) R^(D42) L_(C67) R^(D67) R^(D67) L_(C259) R^(D4) R^(D58) L_(C451) R^(D50) R^(D133) L_(C643) R^(D145) R^(D43) L_(C68) R^(D68) R^(D68) L_(C260) R^(D4) R^(D59) L_(C452) R^(D50) R^(D134) L_(C644) R^(D145) R^(D48) L_(C69) R^(D69) R^(D69) L_(C261) R^(D4) R^(D78) L_(C453) R^(D50) R^(D135) L_(C645) R^(D145) R^(D49) L_(C70) R^(D70) R^(D70) L_(C262) R^(D4) R^(D79) L_(C454) R^(D50) R^(D136) L_(C646) R^(D145) R^(D54) L_(C71) R^(D71) R^(D71) L_(C263) R^(D4) R^(D81) L_(C455) R^(D50) R^(D143) L_(C647) R^(D145) R^(D58) L_(C72) R^(D72) R^(D72) L_(C264) R^(D4) R^(D87) L_(C456) R^(D50) R^(D144) L_(C648) R^(D145) R^(D59) L_(C73) R^(D73) R^(D73) L_(C265) R^(D4) R^(D88) L_(C457) R^(D50) R^(D145) L_(C649) R^(D145) R^(D78) L_(C74) R^(D74) R^(D74) L_(C266) R^(D4) R^(D89) L_(C458) R^(D50) R^(D146) L_(C650) R^(D145) R^(D79) L_(C75) R^(D75) R^(D75) L_(C267) R^(D4) R^(D93) L_(C459) R^(D50) R^(D147) L_(C651) R^(D145) R^(D81) L_(C76) R^(D76) R^(D76) L_(C268) R^(D4) R^(D116) L_(C460) R^(D50) R^(D149) L_(C652) R^(D145) R^(D87) L_(C77) R^(D77) R^(D77) L_(C269) R^(D4) R^(D117) L_(C461) R^(D50) R^(D151) L_(C653) R^(D145) R^(D88) L_(C78) R^(D78) R^(D78) L_(C270) R^(D4) R^(D118) L_(C462) R^(D50) R^(D154) L_(C654) R^(D145) R^(D89) L_(C79) R^(D79) R^(D79) L_(C271) R^(D4) R^(D119) L_(C463) R^(D50) R^(D155) L_(C655) R^(D145) R^(D93) L_(C80) R^(D80) R^(D80) L_(C272) R^(D4) R^(D120) L_(C464) R^(D50) R^(D161) L_(C656) R^(D145) R^(D116) L_(C81) R^(D81) R^(D81) L_(C273) R^(D4) R^(D133) L_(C465) R^(D50) R^(D175) L_(C657) R^(D145) R^(D117) L_(C82) R^(D82) R^(D82) L_(C274) R^(D4) R^(D134) L_(C466) R^(D55) R^(D3) L_(C658) R^(D145) R^(D118) L_(C83) R^(D83) R^(D83) L_(C275) R^(D4) R^(D135) L_(C467) R^(D55) R^(D5) L_(C659) R^(D145) R^(D119) L_(C84) R^(D84) R^(D84) L_(C276) R^(D4) R^(D136) L_(C468) R^(D55) R^(D18) L_(C660) R^(D145) R^(D120) L_(C85) R^(D85) R^(D85) L_(C277) R^(D4) R^(D143) L_(C469) R^(D55) R^(D20) L_(C661) R^(D145) R^(D133) L_(C86) R^(D86) R^(D86) L_(C278) R^(D4) R^(D144) L_(C470) R^(D55) R^(D22) L_(C662) R^(D145) R^(D134) L_(C87) R^(D87) R^(D87) L_(C279) R^(D4) R^(D145) L_(C471) R^(D55) R^(D37) L_(C663) R^(D145) R^(D135) L_(C88) R^(D88) R^(D88) L_(C280) R^(D4) R^(D146) L_(C472) R^(D55) R^(D40) L_(C664) R^(D145) R^(D136) L_(C89) R^(D89) R^(D89) L_(C281) R^(D4) R^(D147) L_(C473) R^(D55) R^(D41) L_(C665) R^(D145) R^(D146) L_(C90) R^(D90) R^(D90) L_(C282) R^(D4) R^(D149) L_(C474) R^(D55) R^(D42) L_(C666) R^(D145) R^(D147) L_(C91) R^(D91) R^(D91) L_(C283) R^(D4) R^(D151) L_(C475) R^(D55) R^(D43) L_(C667) R^(D145) R^(D149) L_(C92) R^(D92) R^(D92) L_(C284) R^(D4) R^(D154) L_(C476) R^(D55) R^(D48) L_(C668) R^(D145) R^(D151) L_(C93) R^(D93) R^(D93) L_(C285) R^(D4) R^(D155) L_(C477) R^(D55) R^(D49) L_(C669) R^(D145) R^(D154) L_(C94) R^(D94) R^(D94) L_(C286) R^(D4) R^(D161) L_(C478) R^(D55) R^(D54) L_(C670) R^(D145) R^(D155) L_(C95) R^(D95) R^(D95) L_(C287) R^(D4) R^(D175) L_(C479) R^(D55) R^(D58) L_(C671) R^(D145) R^(D161) L_(C96) R^(D96) R^(D96) L_(C288) R^(D9) R^(D3) L_(C480) R^(D55) R^(D59) L_(C672) R^(D145) R^(D175) L_(C97) R^(D97) R^(D97) L_(C289) R^(D9) R^(D5) L_(C481) R^(D55) R^(D78) L_(C673) R^(D146) R^(D3) L_(C98) R^(D98) R^(D98) L_(C290) R^(D9) R^(D10) L_(C482) R^(D55) R^(D79) L_(C674) R^(D146) R^(D5) L_(C99) R^(D99) R^(D99) L_(C291) R^(D9) R^(D17) L_(C483) R^(D55) R^(D81) L_(C675) R^(D146) R^(D17) L_(C100) R^(D100) R^(D100) L_(C292) R^(D9) R^(D18) L_(C484) R^(D55) R^(D87) L_(C676) R^(D146) R^(D18) L_(C101) R^(D101) R^(D101) L_(C293) R^(D9) R^(D20) L_(C485) R^(D55) R^(D88) L_(C677) R^(D146) R^(D20) L_(C102) R^(D102) R^(D102) L_(C294) R^(D9) R^(D22) L_(C486) R^(D55) R^(D89) L_(C678) R^(D146) R^(D22) L_(C103) R^(D103) R^(D103) L_(C295) R^(D9) R^(D37) L_(C487) R^(D55) R^(D93) L_(C679) R^(D146) R^(D37) L_(C104) R^(D104) R^(D104) L_(C296) R^(D9) R^(D40) L_(C488) R^(D55) R^(D116) L_(C680) R^(D146) R^(D40) L_(C105) R^(D105) R^(D105) L_(C297) R^(D9) R^(D41) L_(C489) R^(D55) R^(D117) L_(C681) R^(D146) R^(D41) L_(C106) R^(D106) R^(D106) L_(C298) R^(D9) R^(D42) L_(C490) R^(D55) R^(D118) L_(C682) R^(D146) R^(D42) L_(C107) R^(D107) R^(D107) L_(C299) R^(D9) R^(D43) L_(C491) R^(D55) R^(D119) L_(C683) R^(D146) R^(D43) L_(C108) R^(D108) R^(D108) L_(C300) R^(D9) R^(D48) L_(C492) R^(D55) R^(D120) L_(C684) R^(D146) R^(D48) L_(C109) R^(D109) R^(D109) L_(C301) R^(D9) R^(D49) L_(C493) R^(D55) R^(D133) L_(C685) R^(D146) R^(D49) L_(C110) R^(D110) R^(D110) L_(C302) R^(D9) R^(D50) L_(C494) R^(D55) R^(D134) L_(C686) R^(D146) R^(D54) L_(C111) R^(D111) R^(D111) L_(C303) R^(D9) R^(D54) L_(C495) R^(D55) R^(D135) L_(C687) R^(D146) R^(D58) L_(C112) R^(D112) R^(D112) L_(C304) R^(D9) R^(D55) L_(C496) R^(D55) R^(D136) L_(C688) R^(D146) R^(D59) L_(C113) R^(D113) R^(D113) L_(C305) R^(D9) R^(D58) L_(C497) R^(D55) R^(D143) L_(C689) R^(D146) R^(D78) L_(C114) R^(D114) R^(D114) L_(C306) R^(D9) R^(D59) L_(C498) R^(D55) R^(D144) L_(C690) R^(D146) R^(D79) L_(C115) R^(D115) R^(D115) L_(C307) R^(D9) R^(D78) L_(C499) R^(D55) R^(D145) L_(C691) R^(D146) R^(D81) L_(C116) R^(D116) R^(D116) L_(C308) R^(D9) R^(D79) L_(C500) R^(D55) R^(D146) L_(C692) R^(D146) R^(D87) L_(C117) R^(D117) R^(D117) L_(C309) R^(D9) R^(D81) L_(C501) R^(D55) R^(D147) L_(C693) R^(D146) R^(D88) L_(C118) R^(D118) R^(D118) L_(C310) R^(D9) R^(D87) L_(C502) R^(D55) R^(D149) L_(C694) R^(D146) R^(D89) L_(C119) R^(D119) R^(D119) L_(C311) R^(D9) R^(D88) L_(C503) R^(D55) R^(D151) L_(C695) R^(D146) R^(D93) L_(C120) R^(D120) R^(D120) L_(C312) R^(D9) R^(D89) L_(C504) R^(D55) R^(D154) L_(C696) R^(D146) R^(D117) L_(C121) R^(D121) R^(D121) L_(C313) R^(D9) R^(D95) L_(C505) R^(D55) R^(D155) L_(C697) R^(D146) R^(D118) L_(C122) R^(D122) R^(D122) L_(C314) R^(D9) R^(D116) L_(C506) R^(D55) R^(D161) L_(C698) R^(D146) R^(D119) L_(C123) R^(D123) R^(D123) L_(C315) R^(D9) R^(D117) L_(C507) R^(D55) R^(D175) L_(C699) R^(D146) R^(D120) L_(C124) R^(D124) R^(D124) L_(C316) R^(D9) R^(D118) L_(C508) R^(D116) R^(D3) L_(C700) R^(D146) R^(D133) L_(C125) R^(D125) R^(D125) L_(C317) R^(D9) R^(D119) L_(C509) R^(D116) R^(D5) L_(C701) R^(D146) R^(D134) L_(C126) R^(D126) R^(D126) L_(C318) R^(D9) R^(D120) L_(C510) R^(D116) R^(D17) L_(C702) R^(D146) R^(D135) L_(C127) R^(D127) R^(D127) L_(C319) R^(D9) R^(D133) L_(C511) R^(D116) R^(D18) L_(C703) R^(D146) R^(D136) L_(C128) R^(D128) R^(D128) L_(C320) R^(D9) R^(D134) L_(C512) R^(D116) R^(D20) L_(C704) R^(D146) R^(D146) L_(C129) R^(D129) R^(D129) L_(C321) R^(D9) R^(D135) L_(C513) R^(D116) R^(D22) L_(C705) R^(D146) R^(D147) L_(C130) R^(D130) R^(D130) L_(C322) R^(D9) R^(D136) L_(C514) R^(D116) R^(D37) L_(C706) R^(D146) R^(D149) L_(C131) R^(D131) R^(D131) L_(C323) R^(D9) R^(D143) L_(C515) R^(D116) R^(D40) L_(C707) R^(D146) R^(D151) L_(C132) R^(D132) R^(D132) L_(C324) R^(D9) R^(D144) L_(C516) R^(D116) R^(D41) L_(C708) R^(D146) R^(D154) L_(C133) R^(D133) R^(D133) L_(C325) R^(D9) R^(D145) L_(C517) R^(D116) R^(D42) L_(C709) R^(D146) R^(D155) L_(C134) R^(D134) R^(D134) L_(C326) R^(D9) R^(D146) L_(C518) R^(D116) R^(D43) L_(C710) R^(D146) R^(D161) L_(C135) R^(D135) R^(D135) L_(C327) R^(D9) R^(D147) L_(C519) R^(D116) R^(D48) L_(C711) R^(D146) R^(D175) L_(C136) R^(D136) R^(D136) L_(C328) R^(D9) R^(D149) L_(C520) R^(D116) R^(D49) L_(C712) R^(D133) R^(D3) L_(C137) R^(D137) R^(D137) L_(C329) R^(D9) R^(D151) L_(C521) R^(D116) R^(D54) L_(C713) R^(D133) R^(D5) L_(C138) R^(D138) R^(D138) L_(C330) R^(D9) R^(D154) L_(C522) R^(D116) R^(D58) L_(C714) R^(D133) R^(D3) L_(C139) R^(D139) R^(D139) L_(C331) R^(D9) R^(D155) L_(C523) R^(D116) R^(D59) L_(C715) R^(D133) R^(D18) L_(C140) R^(D140) R^(D140) L_(C332) R^(D9) R^(D161) L_(C524) R^(D116) R^(D78) L_(C716) R^(D133) R^(D20) L_(C141) R^(D141) R^(D141) L_(C333) R^(D9) R^(D175) L_(C525) R^(D116) R^(D79) L_(C717) R^(D133) R^(D22) L_(C142) R^(D142) R^(D142) L_(C334) R^(D10) R^(D3) L_(C526) R^(D116) R^(D81) L_(C718) R^(D133) R^(D37) L_(C143) R^(D143) R^(D143) L_(C335) R^(D10) R^(D5) L_(C527) R^(D116) R^(D87) L_(C719) R^(D133) R^(D40) L_(C144) R^(D144) R^(D144) L_(C336) R^(D10) R^(D17) L_(C528) R^(D116) R^(D88) L_(C720) R^(D133) R^(D41) L_(C145) R^(D145) R^(D145) L_(C337) R^(D10) R^(D18) L_(C529) R^(D116) R^(D89) L_(C721) R^(D133) R^(D42) L_(C146) R^(D146) R^(D146) L_(C338) R^(D10) R^(D20) L_(C530) R^(D116) R^(D93) L_(C722) R^(D133) R^(D43) L_(C147) R^(D147) R^(D147) L_(C339) R^(D10) R^(D22) L_(C531) R^(D116) R^(D117) L_(C723) R^(D133) R^(D48) L_(C148) R^(D148) R^(D148) L_(C340) R^(D10) R^(D37) L_(C532) R^(D116) R^(D118) L_(C724) R^(D133) R^(D49) L_(C149) R^(D149) R^(D149) L_(C341) R^(D10) R^(D40) L_(C533) R^(D116) R^(D119) L_(C725) R^(D133) R^(D54) L_(C150) R^(D150) R^(D150) L_(C342) R^(D10) R^(D41) L_(C534) R^(D116) R^(D120) L_(C726) R^(D133) R^(D58) L_(C151) R^(D151) R^(D151) L_(C343) R^(D10) R^(D42) L_(C535) R^(D116) R^(D133) L_(C727) R^(D133) R^(D59) L_(C152) R^(D152) R^(D152) L_(C344) R^(D10) R^(D43) L_(C536) R^(D116) R^(D134) L_(C728) R^(D133) R^(D78) L_(C153) R^(D153) R^(D153) L_(C345) R^(D10) R^(D48) L_(C537) R^(D116) R^(D135) L_(C729) R^(D133) R^(D79) L_(C154) R^(D154) R^(D154) L_(C346) R^(D10) R^(D49) L_(C538) R^(D116) R^(D136) L_(C730) R^(D133) R^(D81) L_(C155) R^(D155) R^(D155) L_(C347) R^(D10) R^(D50) L_(C539) R^(D116) R^(D143) L_(C731) R^(D133) R^(D87) L_(C156) R^(D156) R^(D156) L_(C348) R^(D10) R^(D54) L_(C540) R^(D116) R^(D144) L_(C732) R^(D133) R^(D88) L_(C157) R^(D157) R^(D157) L_(C349) R^(D10) R^(D55) L_(C541) R^(D116) R^(D145) L_(C733) R^(D133) R^(D89) L_(C158) R^(D158) R^(D158) L_(C350) R^(D10) R^(D58) L_(C542) R^(D116) R^(D146) L_(C734) R^(D133) R^(D93) L_(C159) R^(D159) R^(D159) L_(C351) R^(D10) R^(D59) L_(C543) R^(D116) R^(D147) L_(C735) R^(D133) R^(D117) L_(C160) R^(D160) R^(D160) L_(C352) R^(D10) R^(D78) L_(C544) R^(D116) R^(D149) L_(C736) R^(D133) R^(D118) L_(C161) R^(D161) R^(D161) L_(C353) R^(D10) R^(D79) L_(C545) R^(D116) R^(D151) L_(C737) R^(D133) R^(D119) L_(C162) R^(D162) R^(D162) L_(C354) R^(D10) R^(D81) L_(C546) R^(D116) R^(D154) L_(C738) R^(D133) R^(D120) L_(C163) R^(D163) R^(D163) L_(C355) R^(D10) R^(D87) L_(C547) R^(D116) R^(D155) L_(C739) R^(D133) R^(D133) L_(C164) R^(D164) R^(D164) L_(C356) R^(D10) R^(D88) L_(C548) R^(D116) R^(D161) L_(C740) R^(D133) R^(D134) L_(C165) R^(D165) R^(D165) L_(C357) R^(D10) R^(D89) L_(C549) R^(D116) R^(D175) L_(C741) R^(D133) R^(D135) L_(C166) R^(D166) R^(D166) L_(C358) R^(D10) R^(D93) L_(C550) R^(D143) R^(D3) L_(C742) R^(D133) R^(D136) L_(C167) R^(D167) R^(D167) L_(C359) R^(D10) R^(D116) L_(C551) R^(D143) R^(D5) L_(C743) R^(D133) R^(D146) L_(C168) R^(D168) R^(D168) L_(C360) R^(D10) R^(D117) L_(C552) R^(D143) R^(D17) L_(C744) R^(D133) R^(D147) L_(C169) R^(D169) R^(D169) L_(C361) R^(D10) R^(D118) L_(C553) R^(D143) R^(D18) L_(C745) R^(D133) R^(D149) L_(C170) R^(D170) R^(D170) L_(C362) R^(D10) R^(D119) L_(C554) R^(D143) R^(D20) L_(C746) R^(D133) R^(D151) L_(C171) R^(D171) R^(D171) L_(C363) R^(D10) R^(D120) L_(C555) R^(D143) R^(D22) L_(C747) R^(D133) R^(D154) L_(C172) R^(D172) R^(D172) L_(C364) R^(D10) R^(D133) L_(C556) R^(D143) R^(D37) L_(C748) R^(D133) R^(D155) L_(C173) R^(D173) R^(D173) L_(C365) R^(D10) R^(D134) L_(C557) R^(D143) R^(D40) L_(C749) R^(D133) R^(D161) L_(C174) R^(D174) R^(D174) L_(C366) R^(D10) R^(D135) L_(C558) R^(D143) R^(D41) L_(C750) R^(D133) R^(D175) L_(C175) R^(D175) R^(D175) L_(C367) R^(D10) R^(D136) L_(C559) R^(D143) R^(D42) L_(C751) R^(D175) R^(D3) L_(C176) R^(D176) R^(D176) L_(C368) R^(D10) R^(D143) L_(C560) R^(D143) R^(D43) L_(C752) R^(D175) R^(D5) L_(C177) R^(D177) R^(D177) L_(C369) R^(D10) R^(D144) L_(C561) R^(D143) R^(D48) L_(C753) R^(D175) R^(D18) L_(C178) R^(D178) R^(D178) L_(C370) R^(D10) R^(D145) L_(C562) R^(D143) R^(D49) L_(C754) R^(D175) R^(D20) L_(C179) R^(D179) R^(D179) L_(C371) R^(D10) R^(D146) L_(C563) R^(D143) R^(D54) L_(C755) R^(D175) R^(D22) L_(C180) R^(D180) R^(D180) L_(C372) R^(D10) R^(D147) L_(C564) R^(D143) R^(D58) L_(C756) R^(D175) R^(D37) L_(C181) R^(D181) R^(D181) L_(C373) R^(D10) R^(D149) L_(C565) R^(D143) R^(D59) L_(C757) R^(D175) R^(D40) L_(C182) R^(D182) R^(D182) L_(C374) R^(D10) R^(D151) L_(C566) R^(D143) R^(D78) L_(C758) R^(D175) R^(D41) L_(C183) R^(D183) R^(D183) L_(C375) R^(D10) R^(D154) L_(C567) R^(D143) R^(D79) L_(C759) R^(D175) R^(D42) L_(C184) R^(D184) R^(D184) L_(C376) R^(D10) R^(D155) L_(C568) R^(D143) R^(D81) L_(C760) R^(D175) R^(D43) L_(C185) R^(D185) R^(D185) L_(C377) R^(D10) R^(D161) L_(C569) R^(D143) R^(D87) L_(C761) R^(D175) R^(D48) L_(C186) R^(D186) R^(D186) L_(C378) R^(D10) R^(D175) L_(C570) R^(D143) R^(D88) L_(C762) R^(D175) R^(D49) L_(C187) R^(D187) R^(D187) L_(C379) R^(D17) R^(D3) L_(C571) R^(D143) R^(D89) L_(C763) R^(D175) R^(D54) L_(C188) R^(D188) R^(D188) L_(C380) R^(D17) R^(D5) L_(C572) R^(D143) R^(D93) L_(C764) R^(D175) R^(D58) L_(C189) R^(D189) R^(D189) L_(C381) R^(D17) R^(D18) L_(C573) R^(D143) R^(D116) L_(C765) R^(D175) R^(D59) L_(C190) R^(D190) R^(D190) L_(C382) R^(D17) R^(D20) L_(C574) R^(D143) R^(D117) L_(C766) R^(D175) R^(D78) L_(C191) R^(D191) R^(D191) L_(C383) R^(D17) R^(D22) L_(C575) R^(D143) R^(D118) L_(C767) R^(D175) R^(D79) L_(C192) R^(D192) R^(D192) L_(C384) R^(D17) R^(D37) L_(C576) R^(D143) R^(D119) L_(C768) R^(D175) R^(D81) L_(C769) R^(D193) R^(D193) L_(C877) R^(D1) R^(D193) L_(C985) R^(D4) R^(D193) L_(C1093) R^(D9) R^(D193) L_(C770) R^(D194) R^(D194) L_(C878) R^(D1) R^(D194) L_(C986) R^(D4) R^(D194) L_(C1094) R^(D9) R^(D194) L_(C771) R^(D195) R^(D195) L_(C879) R^(D1) R^(D195) L_(C987) R^(D4) R^(D195) L_(C1095) R^(D9) R^(D195) L_(C772) R^(D196) R^(D196) L_(C880) R^(D1) R^(D196) L_(C988) R^(D4) R^(D196) L_(C1096) R^(D9) R^(D196) L_(C773) R^(D197) R^(D197) L_(C881) R^(D1) R^(D197) L_(C989) R^(D4) R^(D197) L_(C1097) R^(D9) R^(D197) L_(C774) R^(D198) R^(D198) L_(C882) R^(D1) R^(D198) L_(C990) R^(D4) R^(D198) L_(C1098) R^(D9) R^(D198) L_(C775) R^(D199) R^(D199) L_(C883) R^(D1) R^(D199) L_(C991) R^(D4) R^(D199) L_(C1099) R^(D9) R^(D199) L_(C776) R^(D200) R^(D200) L_(C884) R^(D1) R^(D200) L_(C992) R^(D4) R^(D200) L_(C1100) R^(D9) R^(D200) L_(C777) R^(D201) R^(D201) L_(C885) R^(D1) R^(D201) L_(C993) R^(D4) R^(D201) L_(C1101) R^(D9) R^(D201) L_(C778) R^(D202) R^(D202) L_(C886) R^(D1) R^(D202) L_(C994) R^(D4) R^(D202) L_(C1102) R^(D9) R^(D202) L_(C779) R^(D203) R^(D203) L_(C887) R^(D1) R^(D203) L_(C995) R^(D4) R^(D203) L_(C1103) R^(D9) R^(D203) L_(C780) R^(D204) R^(D204) L_(C888) R^(D1) R^(D204) L_(C996) R^(D4) R^(D204) L_(C1104) R^(D9) R^(D204) L_(C781) R^(D205) R^(D205) L_(C889) R^(D1) R^(D205) L_(C997) R^(D4) R^(D205) L_(C1105) R^(D9) R^(D205) L_(C782) R^(D206) R^(D206) L_(C890) R^(D1) R^(D206) L_(C998) R^(D4) R^(D206) L_(C1106) R^(D9) R^(D206) L_(C783) R^(D207) R^(D207) L_(C891) R^(D1) R^(D207) L_(C999) R^(D4) R^(D207) L_(C1107) R^(D9) R^(D207) L_(C784) R^(D208) R^(D208) L_(C892) R^(D1) R^(D208) L_(C1000) R^(D4) R^(D208) L_(C1108) R^(D9) R^(D208) L_(C785) R^(D209) R^(D209) L_(C893) R^(D1) R^(D209) L_(C1001) R^(D4) R^(D209) L_(C1109) R^(D9) R^(D209) L_(C786) R^(D210) R^(D210) L_(C894) R^(D1) R^(D210) L_(C1002) R^(D4) R^(D210) L_(C1110) R^(D9) R^(D210) L_(C787) R^(D211) R^(D211) L_(C895) R^(D1) R^(D211) L_(C1003) R^(D4) R^(D211) L_(C1111) R^(D9) R^(D211) L_(C788) R^(D212) R^(D212) L_(C896) R^(D1) R^(D212) L_(C1004) R^(D4) R^(D212) L_(C1112) R^(D9) R^(D212) L_(C789) R^(D213) R^(D213) L_(C897) R^(D1) R^(D213) L_(C1005) R^(D4) R^(D213) L_(C1113) R^(D9) R^(D213) L_(C790) R^(D214) R^(D214) L_(C898) R^(D1) R^(D214) L_(C1006) R^(D4) R^(D214) L_(C1114) R^(D9) R^(D214) L_(C791) R^(D215) R^(D215) L_(C899) R^(D1) R^(D215) L_(C1007) R^(D4) R^(D215) L_(C1115) R^(D9) R^(D215) L_(C792) R^(D216) R^(D216) L_(C900) R^(D1) R^(D216) L_(C1008) R^(D4) R^(D216) L_(C1116) R^(D9) R^(D216) L_(C793) R^(D217) R^(D217) L_(C901) R^(D1) R^(D217) L_(C1009) R^(D4) R^(D217) L_(C1117) R^(D9) R^(D217) L_(C794) R^(D218) R^(D218) L_(C902) R^(D1) R^(D218) L_(C1010) R^(D4) R^(D218) L_(C1118) R^(D9) R^(D218) L_(C795) R^(D219) R^(D219) L_(C903) R^(D1) R^(D219) L_(C1011) R^(D4) R^(D219) L_(C1119) R^(D9) R^(D219) L_(C796) R^(D220) R^(D220) L_(C904) R^(D1) R^(D220) L_(C1012) R^(D4) R^(D220) L_(C1120) R^(D9) R^(D220) L_(C797) R^(D221) R^(D221) L_(C905) R^(D1) R^(D221) L_(C1013) R^(D4) R^(D221) L_(C1121) R^(D9) R^(D221) L_(C798) R^(D222) R^(D222) L_(C906) R^(D1) R^(D222) L_(C1014) R^(D4) R^(D222) L_(C1122) R^(D9) R^(D222) L_(C799) R^(D223) R^(D223) L_(C907) R^(D1) R^(D223) L_(C1015) R^(D4) R^(D223) L_(C1123) R^(D9) R^(D223) L_(C800) R^(D224) R^(D224) L_(C908) R^(D1) R^(D224) L_(C1016) R^(D4) R^(D224) L_(C1124) R^(D9) R^(D224) L_(C801) R^(D225) R^(D225) L_(C909) R^(D1) R^(D225) L_(C1017) R^(D4) R^(D225) L_(C1125) R^(D9) R^(D225) L_(C802) R^(D226) R^(D226) L_(C910) R^(D1) R^(D226) L_(C1018) R^(D4) R^(D226) L_(C1126) R^(D9) R^(D226) L_(C803) R^(D227) R^(D227) L_(C911) R^(D1) R^(D227) L_(C1019) R^(D4) R^(D227) L_(C1127) R^(D9) R^(D227) L_(C804) R^(D228) R^(D228) L_(C912) R^(D1) R^(D228) L_(C1020) R^(D4) R^(D228) L_(C1128) R^(D9) R^(D228) L_(C805) R^(D229) R^(D229) L_(C913) R^(D1) R^(D229) L_(C1021) R^(D4) R^(D229) L_(C1129) R^(D9) R^(D229) L_(C806) R^(D230) R^(D230) L_(C914) R^(D1) R^(D230) L_(C1022) R^(D4) R^(D230) L_(C1130) R^(D9) R^(D230) L_(C807) R^(D231) R^(D231) L_(C915) R^(D1) R^(D231) L_(C1023) R^(D4) R^(D231) L_(C1131) R^(D9) R^(D231) L_(C808) R^(D232) R^(D232) L_(C916) R^(D1) R^(D232) L_(C1024) R^(D4) R^(D232) L_(C1132) R^(D9) R^(D232) L_(C809) R^(D233) R^(D233) L_(C917) R^(D1) R^(D233) L_(C1025) R^(D4) R^(D233) L_(C1133) R^(D9) R^(D233) L_(C810) R^(D234) R^(D234) L_(C918) R^(D1) R^(D234) L_(C1026) R^(D4) R^(D234) L_(C1134) R^(D9) R^(D234) L_(C811) R^(D235) R^(D235) L_(C919) R^(D1) R^(D235) L_(C1027) R^(D4) R^(D235) L_(C1135) R^(D9) R^(D235) L_(C812) R^(D236) R^(D236) L_(C920) R^(D1) R^(D236) L_(C1028) R^(D4) R^(D236) L_(C1136) R^(D9) R^(D236) L_(C813) R^(D237) R^(D237) L_(C921) R^(D1) R^(D237) L_(C1029) R^(D4) R^(D237) L_(C1137) R^(D9) R^(D237) L_(C814) R^(D238) R^(D238) L_(C922) R^(D1) R^(D238) L_(C1030) R^(D4) R^(D238) L_(C1138) R^(D9) R^(D238) L_(C815) R^(D239) R^(D239) L_(C923) R^(D1) R^(D239) L_(C1031) R^(D4) R^(D239) L_(C1139) R^(D9) R^(D239) L_(C816) R^(D240) R^(D240) L_(C924) R^(D1) R^(D240) L_(C1032) R^(D4) R^(D240) L_(C1140) R^(D9) R^(D240) L_(C817) R^(D241) R^(D241) L_(C925) R^(D1) R^(D241) L_(C1033) R^(D4) R^(D241) L_(C1141) R^(D9) R^(D241) L_(C818) R^(D242) R^(D242) L_(C926) R^(D1) R^(D242) L_(C1034) R^(D4) R^(D242) L_(C1142) R^(D9) R^(D242) L_(C819) R^(D243) R^(D243) L_(C927) R^(D1) R^(D243) L_(C1035) R^(D4) R^(D243) L_(C1143) R^(D9) R^(D243) L_(C820) R^(D244) R^(D244) L_(C928) R^(D1) R^(D244) L_(C1036) R^(D4) R^(D244) L_(C1144) R^(D9) R^(D244) L_(C821) R^(D245) R^(D245) L_(C929) R^(D1) R^(D245) L_(C1037) R^(D4) R^(D245) L_(C1145) R^(D9) R^(D245) L_(C822) R^(D246) R^(D246) L_(C930) R^(D1) R^(D246) L_(C1038) R^(D4) R^(D246) L_(C1146) R^(D9) R^(D246) L_(C823) R^(D17) R^(D193) L_(C931) R^(D50) R^(D193) L_(C1039) R^(D145) R^(D193) L_(C1147) R^(D168) R^(D193) L_(C824) R^(D17) R^(D194) L_(C932) R^(D50) R^(D194) L_(C1040) R^(D145) R^(D194) L_(C1148) R^(D168) R^(D194) L_(C825) R^(D17) R^(D195) L_(C933) R^(D50) R^(D195) L_(C1041) R^(D145) R^(D195) L_(C1149) R^(D168) R^(D195) L_(C826) R^(D17) R^(D196) L_(C934) R^(D50) R^(D196) L_(C1042) R^(D145) R^(D196) L_(C1150) R^(D168) R^(D196) L_(C827) R^(D17) R^(D197) L_(C935) R^(D50) R^(D197) L_(C1043) R^(D145) R^(D197) L_(C1151) R^(D168) R^(D197) L_(C828) R^(D17) R^(D198) L_(C936) R^(D50) R^(D198) L_(C1044) R^(D145) R^(D198) L_(C1152) R^(D168) R^(D198) L_(C829) R^(D17) R^(D199) L_(C937) R^(D50) R^(D199) L_(C1045) R^(D145) R^(D199) L_(C1153) R^(D168) R^(D199) L_(C830) R^(D17) R^(D200) L_(C938) R^(D50) R^(D200) L_(C1046) R^(D145) R^(D200) L_(C1154) R^(D168) R^(D200) L_(C831) R^(D17) R^(D201) L_(C939) R^(D50) R^(D201) L_(C1047) R^(D145) R^(D201) L_(C1155) R^(D168) R^(D201) L_(C832) R^(D17) R^(D202) L_(C940) R^(D50) R^(D202) L_(C1048) R^(D145) R^(D202) L_(C1156) R^(D168) R^(D202) L_(C833) R^(D17) R^(D203) L_(C941) R^(D50) R^(D203) L_(C1049) R^(D145) R^(D203) L_(C1157) R^(D168) R^(D203) L_(C834) R^(D17) R^(D204) L_(C942) R^(D50) R^(D204) L_(C1050) R^(D145) R^(D204) L_(C1158) R^(D168) R^(D204) L_(C835) R^(D17) R^(D205) L_(C943) R^(D50) R^(D205) L_(C1051) R^(D145) R^(D205) L_(C1159) R^(D168) R^(D205) L_(C836) R^(D17) R^(D206) L_(C944) R^(D50) R^(D206) L_(C1052) R^(D145) R^(D206) L_(C1160) R^(D168) R^(D206) L_(C837) R^(D17) R^(D207) L_(C945) R^(D50) R^(D207) L_(C1053) R^(D145) R^(D207) L_(C1161) R^(D168) R^(D207) L_(C838) R^(D17) R^(D208) L_(C946) R^(D50) R^(D208) L_(C1054) R^(D145) R^(D208) L_(C1162) R^(D168) R^(D208) L_(C839) R^(D17) R^(D209) L_(C947) R^(D50) R^(D209) L_(C1055) R^(D145) R^(D209) L_(C1163) R^(D168) R^(D209) L_(C840) R^(D17) R^(D210) L_(C948) R^(D50) R^(D210) L_(C1056) R^(D145) R^(D210) L_(C1164) R^(D168) R^(D210) L_(C841) R^(D17) R^(D211) L_(C949) R^(D50) R^(D211) L_(C1057) R^(D145) R^(D211) L_(C1165) R^(D168) R^(D211) L_(C842) R^(D17) R^(D212) L_(C950) R^(D50) R^(D212) L_(C1058) R^(D145) R^(D212) L_(C1166) R^(D168) R^(D212) L_(C843) R^(D17) R^(D213) L_(C951) R^(D50) R^(D213) L_(C1059) R^(D145) R^(D213) L_(C1167) R^(D168) R^(D213) L_(C844) R^(D17) R^(D214) L_(C952) R^(D50) R^(D214) L_(C1060) R^(D145) R^(D214) L_(C1168) R^(D168) R^(D214) L_(C845) R^(D17) R^(D215) L_(C953) R^(D50) R^(D215) L_(C1061) R^(D145) R^(D215) L_(C1169) R^(D168) R^(D215) L_(C846) R^(D17) R^(D216) L_(C954) R^(D50) R^(D216) L_(C1062) R^(D145) R^(D216) L_(C1170) R^(D168) R^(D216) L_(C847) R^(D17) R^(D217) L_(C955) R^(D50) R^(D217) L_(C1063) R^(D145) R^(D217) L_(C1171) R^(D168) R^(D217) L_(C848) R^(D17) R^(D218) L_(C956) R^(D50) R^(D218) L_(C1064) R^(D145) R^(D218) L_(C1172) R^(D168) R^(D218) L_(C849) R^(D17) R^(D219) L_(C957) R^(D50) R^(D219) L_(C1065) R^(D145) R^(D219) L_(C1173) R^(D168) R^(D219) L_(C850) R^(D17) R^(D220) L_(C958) R^(D50) R^(D220) L_(C1066) R^(D145) R^(D220) L_(C1174) R^(D168) R^(D220) L_(C851) R^(D17) R^(D221) L_(C959) R^(D50) R^(D221) L_(C1067) R^(D145) R^(D221) L_(C1175) R^(D168) R^(D221) L_(C852) R^(D17) R^(D222) L_(C960) R^(D50) R^(D222) L_(C1068) R^(D145) R^(D222) L_(C1176) R^(D168) R^(D222) L_(C853) R^(D17) R^(D223) L_(C961) R^(D50) R^(D223) L_(C1069) R^(D145) R^(D223) L_(C1177) R^(D168) R^(D223) L_(C854) R^(D17) R^(D224) L_(C962) R^(D50) R^(D224) L_(C1070) R^(D145) R^(D224) L_(C1178) R^(D168) R^(D224) L_(C855) R^(D17) R^(D225) L_(C963) R^(D50) R^(D225) L_(C1071) R^(D145) R^(D225) L_(C1179) R^(D168) R^(D225) L_(C856) R^(D17) R^(D226) L_(C964) R^(D50) R^(D226) L_(C1072) R^(D145) R^(D226) L_(C1180) R^(D168) R^(D226) L_(C857) R^(D17) R^(D227) L_(C965) R^(D50) R^(D227) L_(C1073) R^(D145) R^(D227) L_(C1181) R^(D168) R^(D227) L_(C858) R^(D17) R^(D228) L_(C966) R^(D50) R^(D228) L_(C1074) R^(D145) R^(D228) L_(C1182) R^(D168) R^(D228) L_(C859) R^(D17) R^(D229) L_(C967) R^(D50) R^(D229) L_(C1075) R^(D145) R^(D229) L_(C1183) R^(D168) R^(D229) L_(C860) R^(D17) R^(D230) L_(C968) R^(D50) R^(D230) L_(C1076) R^(D145) R^(D230) L_(C1184) R^(D168) R^(D230) L_(C861) R^(D17) R^(D231) L_(C969) R^(D50) R^(D231) L_(C1077) R^(D145) R^(D231) L_(C1185) R^(D168) R^(D231) L_(C862) R^(D17) R^(D232) L_(C970) R^(D50) R^(D232) L_(C1078) R^(D145) R^(D232) L_(C1186) R^(D168) R^(D232) L_(C863) R^(D17) R^(D233) L_(C971) R^(D50) R^(D233) L_(C1079) R^(D145) R^(D233) L_(C1187) R^(D168) R^(D233) L_(C864) R^(D17) R^(D234) L_(C972) R^(D50) R^(D234) L_(C1080) R^(D145) R^(D234) L_(C1188) R^(D168) R^(D234) L_(C865) R^(D17) R^(D235) L_(C973) R^(D50) R^(D235) L_(C1081) R^(D145) R^(D235) L_(C1189) R^(D168) R^(D235) L_(C866) R^(D17) R^(D236) L_(C974) R^(D50) R^(D236) L_(C1082) R^(D145) R^(D236) L_(C1190) R^(D168) R^(D236) L_(C867) R^(D17) R^(D237) L_(C975) R^(D50) R^(D237) L_(C1083) R^(D145) R^(D237) L_(C1191) R^(D168) R^(D237) L_(C868) R^(D17) R^(D238) L_(C976) R^(D50) R^(D238) L_(C1084) R^(D145) R^(D238) L_(C1192) R^(D168) R^(D238) L_(C869) R^(D17) R^(D239) L_(C977) R^(D50) R^(D239) L_(C1085) R^(D145) R^(D239) L_(C1193) R^(D168) R^(D239) L_(C870) R^(D17) R^(D240) L_(C978) R^(D50) R^(D240) L_(C1086) R^(D145) R^(D240) L_(C1194) R^(D168) R^(D240) L_(C871) R^(D17) R^(D241) L_(C979) R^(D50) R^(D241) L_(C1087) R^(D145) R^(D241) L_(C1195) R^(D168) R^(D241) L_(C872) R^(D17) R^(D242) L_(C980) R^(D50) R^(D242) L_(C1088) R^(D145) R^(D242) L_(C1196) R^(D168) R^(D242) L_(C873) R^(D17) R^(D243) L_(C981) R^(D50) R^(D243) L_(C1089) R^(D145) R^(D243) L_(C1197) R^(D168) R^(D243) L_(C874) R^(D17) R^(D244) L_(C982) R^(D50) R^(D244) L_(C1090) R^(D145) R^(D244) L_(C1198) R^(D168) R^(D244) L_(C875) R^(D17) R^(D245) L_(C983) R^(D50) R^(D245) L_(C1091) R^(D145) R^(D245) L_(C1199) R^(D168) R^(D245) L_(C876) R^(D17) R^(D246) L_(C984) R^(D50) R^(D246) L_(C1092) R^(D145) R^(D246) L_(C1200) R^(D168) R^(D246) L_(C1201) R^(D10) R^(D193) L_(C1255) R^(D55) R^(D193) L_(C1309) R^(D37) R^(D193) L_(C1363) R^(D143) R^(D193) L_(C1202) R^(D10) R^(D194) L_(C1256) R^(D55) R^(D194) L_(C1310) R^(D37) R^(D194) L_(C1364) R^(D143) R^(D194) L_(C1203) R^(D10) R^(D195) L_(C1257) R^(D55) R^(D195) L_(C1311) R^(D37) R^(D195) L_(C1365) R^(D143) R^(D195) L_(C1204) R^(D10) R^(D196) L_(C1258) R^(D55) R^(D196) L_(C1312) R^(D37) R^(D196) L_(C1366) R^(D143) R^(D196) L_(C1205) R^(D10) R^(D197) L_(C1259) R^(D55) R^(D197) L_(C1313) R^(D37) R^(D197) L_(C1367) R^(D143) R^(D197) L_(C1206) R^(D10) R^(D198) L_(C1260) R^(D55) R^(D198) L_(C1314) R^(D37) R^(D198) L_(C1368) R^(D143) R^(D198) L_(C1207) R^(D10) R^(D199) L_(C1261) R^(D55) R^(D199) L_(C1315) R^(D37) R^(D199) L_(C1369) R^(D143) R^(D199) L_(C1208) R^(D10) R^(D200) L_(C1262) R^(D55) R^(D200) L_(C1316) R^(D37) R^(D200) L_(C1370) R^(D143) R^(D200) L_(C1209) R^(D10) R^(D201) L_(C1263) R^(D55) R^(D201) L_(C1317) R^(D37) R^(D201) L_(C1371) R^(D143) R^(D201) L_(C1210) R^(D10) R^(D202) L_(C1264) R^(D55) R^(D202) L_(C1318) R^(D37) R^(D202) L_(C1372) R^(D143) R^(D202) L_(C1211) R^(D10) R^(D203) L_(C1265) R^(D55) R^(D203) L_(C1319) R^(D37) R^(D203) L_(C1373) R^(D143) R^(D203) L_(C1212) R^(D10) R^(D204) L_(C1266) R^(D55) R^(D204) L_(C1320) R^(D37) R^(D204) L_(C1374) R^(D143) R^(D204) L_(C1213) R^(D10) R^(D205) L_(C1267) R^(D55) R^(D205) L_(C1321) R^(D37) R^(D205) L_(C1375) R^(D143) R^(D205) L_(C1214) R^(D10) R^(D206) L_(C1268) R^(D55) R^(D206) L_(C1322) R^(D37) R^(D206) L_(C1376) R^(D143) R^(D206) L_(C1215) R^(D10) R^(D207) L_(C1269) R^(D55) R^(D207) L_(C1323) R^(D37) R^(D207) L_(C1377) R^(D143) R^(D207) L_(C1216) R^(D10) R^(D208) L_(C1270) R^(D55) R^(D208) L_(C1324) R^(D37) R^(D208) L_(C1378) R^(D143) R^(D208) L_(C1217) R^(D10) R^(D209) L_(C1271) R^(D55) R^(D209) L_(C1325) R^(D37) R^(D209) L_(C1379) R^(D143) R^(D209) L_(C1218) R^(D10) R^(D210) L_(C1272) R^(D55) R^(D210) L_(C1326) R^(D37) R^(D210) L_(C1380) R^(D143) R^(D210) L_(C1219) R^(D10) R^(D211) L_(C1273) R^(D55) R^(D211) L_(C1327) R^(D37) R^(D211) L_(C1381) R^(D143) R^(D211) L_(C1220) R^(D10) R^(D212) L_(C1274) R^(D55) R^(D212) L_(C1328) R^(D37) R^(D212) L_(C1382) R^(D143) R^(D212) L_(C1221) R^(D10) R^(D213) L_(C1275) R^(D55) R^(D213) L_(C1329) R^(D37) R^(D213) L_(C1383) R^(D143) R^(D213) L_(C1222) R^(D10) R^(D214) L_(C1276) R^(D55) R^(D214) L_(C1330) R^(D37) R^(D214) L_(C1384) R^(D143) R^(D214) L_(C1223) R^(D10) R^(D215) L_(C1277) R^(D55) R^(D215) L_(C1331) R^(D37) R^(D215) L_(C1385) R^(D143) R^(D215) L_(C1224) R^(D10) R^(D216) L_(C1278) R^(D55) R^(D216) L_(C1332) R^(D37) R^(D216) L_(C1386) R^(D143) R^(D216) L_(C1225) R^(D10) R^(D217) L_(C1279) R^(D55) R^(D217) L_(C1333) R^(D37) R^(D217) L_(C1387) R^(D143) R^(D217) L_(C1226) R^(D10) R^(D218) L_(C1280) R^(D55) R^(D218) L_(C1334) R^(D37) R^(D218) L_(C1388) R^(D143) R^(D218) L_(C1227) R^(D10) R^(D219) L_(C1281) R^(D55) R^(D219) L_(C1335) R^(D37) R^(D219) L_(C1389) R^(D143) R^(D219) L_(C1228) R^(D10) R^(D220) L_(C1282) R^(D55) R^(D220) L_(C1336) R^(D37) R^(D220) L_(C1390) R^(D143) R^(D220) L_(C1229) R^(D10) R^(D221) L_(C1283) R^(D55) R^(D221) L_(C1337) R^(D37) R^(D221) L_(C1391) R^(D143) R^(D221) L_(C1230) R^(D10) R^(D222) L_(C1284) R^(D55) R^(D222) L_(C1338) R^(D37) R^(D222) L_(C1392) R^(D143) R^(D222) L_(C1231) R^(D10) R^(D223) L_(C1285) R^(D55) R^(D223) L_(C1339) R^(D37) R^(D223) L_(C1393) R^(D143) R^(D223) L_(C1232) R^(D10) R^(D224) L_(C1286) R^(D55) R^(D224) L_(C1340) R^(D37) R^(D224) L_(C1394) R^(D143) R^(D224) L_(C1233) R^(D10) R^(D225) L_(C1287) R^(D55) R^(D225) L_(C1341) R^(D37) R^(D225) L_(C1395) R^(D143) R^(D225) L_(C1234) R^(D10) R^(D226) L_(C1288) R^(D55) R^(D226) L_(C1342) R^(D37) R^(D226) L_(C1396) R^(D143) R^(D226) L_(C1235) R^(D10) R^(D227) L_(C1289) R^(D55) R^(D227) L_(C1343) R^(D37) R^(D227) L_(C1397) R^(D143) R^(D227) L_(C1236) R^(D10) R^(D228) L_(C1290) R^(D55) R^(D228) L_(C1344) R^(D37) R^(D228) L_(C1398) R^(D143) R^(D228) L_(C1237) R^(D10) R^(D229) L_(C1291) R^(D55) R^(D229) L_(C1345) R^(D37) R^(D229) L_(C1399) R^(D143) R^(D229) L_(C1238) R^(D10) R^(D230) L_(C1292) R^(D55) R^(D230) L_(C1346) R^(D37) R^(D230) L_(C1400) R^(D143) R^(D230) L_(C1239) R^(D10) R^(D231) L_(C1293) R^(D55) R^(D231) L_(C1347) R^(D37) R^(D231) L_(C1401) R^(D143) R^(D231) L_(C1240) R^(D10) R^(D232) L_(C1294) R^(D55) R^(D232) L_(C1348) R^(D37) R^(D232) L_(C1402) R^(D143) R^(D232) L_(C1241) R^(D10) R^(D233) L_(C1295) R^(D55) R^(D233) L_(C1349) R^(D37) R^(D233) L_(C1403) R^(D143) R^(D233) L_(C1242) R^(D10) R^(D234) L_(C1296) R^(D55) R^(D234) L_(C1350) R^(D37) R^(D234) L_(C1404) R^(D143) R^(D234) L_(C1243) R^(D10) R^(D235) L_(C1297) R^(D55) R^(D235) L_(C1351) R^(D37) R^(D235) L_(C1405) R^(D143) R^(D235) L_(C1244) R^(D10) R^(D236) L_(C1298) R^(D55) R^(D236) L_(C1352) R^(D37) R^(D236) L_(C1406) R^(D143) R^(D236) L_(C1245) R^(D10) R^(D237) L_(C1299) R^(D55) R^(D237) L_(C1353) R^(D37) R^(D237) L_(C1407) R^(D143) R^(D237) L_(C1246) R^(D10) R^(D238) L_(C1300) R^(D55) R^(D238) L_(C1354) R^(D37) R^(D238) L_(C1408) R^(D143) R^(D238) L_(C1247) R^(D10) R^(D239) L_(C1301) R^(D55) R^(D239) L_(C1355) R^(D37) R^(D239) L_(C1409) R^(D143) R^(D239) L_(C1248) R^(D10) R^(D240) L_(C1302) R^(D55) R^(D240) L_(C1356) R^(D37) R^(D240) L_(C1410) R^(D143) R^(D240) L_(C1249) R^(D10) R^(D241) L_(C1303) R^(D55) R^(D241) L_(C1357) R^(D37) R^(D241) L_(C1411) R^(D143) R^(D241) L_(C1250) R^(D10) R^(D242) L_(C1304) R^(D55) R^(D242) L_(C1358) R^(D37) R^(D242) L_(C1412) R^(D143) R^(D242) L_(C1251) R^(D10) R^(D243) L_(C1305) R^(D55) R^(D243) L_(C1359) R^(D37) R^(D243) L_(C1413) R^(D143) R^(D243) L_(C1252) R^(D10) R^(D244) L_(C1306) R^(D55) R^(D244) L_(C1360) R^(D37) R^(D244) L_(C1414) R^(D143) R^(D244) L_(C1253) R^(D10) R^(D245) L_(C1307) R^(D55) R^(D245) L_(C1361) R^(D37) R^(D245) L_(C1415) R^(D143) R^(D245) L_(C1254) R^(D10) R^(D246) L_(C1308) R^(D55) R^(D246) L_(C1362) R^(D37) R^(D246) L_(C1416) R^(D143) R^(D246)

where R^(D1) to R^(D246) have the structures in the following LIST 10:

In some embodiments, the compound has the formula Ir(L_(Ai-m))(L_(Bk))₂ or Ir(L_(Ai-m))₂(L_(Bk)), where the compound is selected from the group consisting of only those compounds having one of the structures of the following LIST 11 for the L_(Bk) ligand: L_(B1), L_(B2), L_(B18), L_(B28), L_(B38), L_(B108), L_(B118), L_(B122), L_(B124), L_(B126), L_(B128), L_(B130), L_(B132), L_(B134), L_(B136), L_(B138), L_(B140), L_(B142), L_(B144), L_(B156), L_(B158), L_(B160), L_(B162), L_(B164), L_(B168), L_(B172), L_(B175), L_(B204), L_(B206), L_(B214), L_(B216), L_(B218), L_(B220), L_(B222), L_(B231), L_(B233), L_(B235), L_(B237), L_(B240), L_(B242), L_(B244), L_(B246), L_(B248), L_(B250), L_(B252), L_(B254), L_(B256), L_(B258), L_(B260), L_(B262), L_(B264), L_(B265), L_(B266), L_(B267), L_(B268), L_(B269), and L_(B270).

In some embodiments, the compound has the formula Ir(L_(Ai-m))(L_(Bk))₂ or Ir(L_(Ai-m))₂(L_(Bk)), where the compound is selected from the group consisting of only those compounds having one of the structures of the following LIST 12 for the L_(Bk) ligand: L_(B1), L_(B2), L_(B18), L_(B28), L_(B38), L_(B108), L_(B118), L_(B122), L_(B126), L_(B128), L_(B132), L_(B136), L_(B138), L_(B142), L_(B156), L_(B162), L_(B204), L_(B206), L_(B214), L_(B216), L_(B218), L_(B220), L_(B231), L_(B233), L_(B 237), L_(B 264), L_(B265), L_(B266), L_(B267), L_(B268), L_(B269), and L_(B270).

In some embodiments, the compound has the formula Ir(L_(Ai-m))₂(L_(Cj-I)) or Ir(L_(Ai-m))₂(L_(Cj-II)), where the compound is selected from the group consisting of only those compounds having L_(Cj-I) or L_(Cj-II) ligand whose corresponding R²⁰¹ and R²⁰² are defined to be one the structures of the following LIST 13:

In some embodiments, the compound has the formula Ir(L_(Ai-m))₂(L_(Cj-I)) or Ir(L_(Ai-m))₂(L_(Cj-II)), where the compound is selected from the group consisting of only those compounds having L_(Cj-I) or L_(Cj-II) ligand whose corresponding R²⁰¹ and R²⁰² are defined to be one of the structures of the following LIST 14:

In some embodiments, the compound has the formula Ir(L_(Ai-m))₂(L_(Cj-I)), and the compound is selected from the group consisting of only those compounds having one of the following structures of the following LIST 15 for the L_(Cj-I) ligand:

In some embodiments, the compound is selected from the group consisting of the structures of the following LIST 16:

In some embodiments, the compound has a structure of Formula II

where:

M¹ is Pd or Pt;

moieties E and F are each independently a monocyclic or polycyclic ring structure comprising 5-membered and/or 6-membered carbocyclic or heterocyclic rings;

Z¹ and Z² are each independently C or N;

K¹ and K² are each independently selected from the group consisting of a direct bond, O, and S, wherein at least one of K, K¹, and K² is a direct bond;

L¹, L², and L³ are each independently selected from the group consisting of a single bond, absent a bond, O, Se, S, SO, SO₂, C═CR′R″, C═NR′, CR′R″, SiR′R″, P(O)R′, BR′, and NR′, wherein at least one of L¹ and L² is present;

X^(3′) and X^(4′) are each independently C or N;

R^(E) and R^(F) each independently represents zero, mono, or up to a maximum allowed substitution to its associated ring;

each of R′, R″, R^(E), and R^(F) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof; and

two of R, R′, R″, R^(A), R^(E), and R^(F), can be joined or fused together to form a ring.

In some embodiments, moiety E and moiety F are both 6-membered aromatic rings.

In some embodiments, moiety F is a 5-membered or 6-membered heteroaromatic ring.

In some embodiments, L¹ is 0 or CR′R″.

In some embodiments, Z² is N and Z¹ is C. In some embodiments, Z² is C and Z¹ is N.

In some embodiments, L² is a direct bond. In some embodiments, L² is NR′.

In some embodiments, K, K¹, and K² are all direct bonds.

In some embodiments, X^(3′) and X^(4′) are both C.

In some embodiments, the compound is selected from the group consisting of the structures of the following LIST 17:

wherein:

ring A1 is a 5-membered or 6-membered carbocyclic or heterocyclic ring;

R^(A1) represents mono to the maximum allowable substitution, or no substitution;

R^(A1) is a hydrogen or a substituent selected from the group consisting of the General Substituents as defined herein;

R^(X) and R^(Y) are each selected from the group consisting of alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, aryl, heteroaryl, and combinations thereof; and

each R^(G) is independently a hydrogen or a substituent selected from the group consisting of the Preferred General Substituents as defined herein.

In some embodiments, the compound is selected from the group consisting of the following LIST 18:

In some embodiments, the compound having a first ligand L_(A) of Formula I described herein can be at least 30% deuterated, at least 40% deuterated, at least 50% deuterated, at least 60% deuterated, at least 70% deuterated, at least 80% deuterated, at least 90% deuterated, at least 95% deuterated, at least 99% deuterated, or 100% deuterated. As used herein, percent deuteration has its ordinary meaning and includes the percent of possible hydrogen atoms (e.g., positions that are hydrogen, deuterium, or halogen) that are replaced by deuterium atoms.

C. The OLEDs and the Devices of the Present Disclosure

In another aspect, the present disclosure also provides an OLED device comprising a first organic layer that contains a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the OLED comprises an anode, a cathode, and a first organic layer disposed between the anode and the cathode. The first organic layer can comprise a compound comprising a first ligand L_(A) of Formula I as defined herein.

In some embodiments, the organic layer may be an emissive layer and the compound as described herein may be an emissive dopant or a non-emissive dopant.

In some embodiments, the organic layer may further comprise a host, wherein the host comprises a triphenylene containing benzo-fused thiophene or benzo-fused furan, wherein any substituent in the host is an unfused substituent independently selected from the group consisting of C_(n)H_(2n+1), OC_(n)H_(2n+1), OAr₁, N(C_(n)H_(2n+1))₂, N(Ar₁)(Ar₂), CH═CH—C_(n)H_(2n+1), C≡CC_(n)H_(2n+1), Ar₁, Ar₁-Ar₂, C_(n)H₂—Ar₁, or no substitution, wherein n is from 1 to 10; and wherein Ar₁ and Ar₂ are independently selected from the group consisting of benzene, biphenyl, naphthalene, triphenylene, carbazole, and heteroaromatic analogs thereof.

In some embodiments, the organic layer may further comprise a host, wherein host comprises at least one chemical group selected from the group consisting of triphenylene, carbazole, indolocarbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, 5λ2-benzo[d]benzo[4,5]imidazo[3,2-a]imidazole, 5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene, triazine, aza-triphenylene, aza-carbazole, aza-indolocarbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene, aza-5λ2-benzo[d]benzo[4,5]imidazo[3,2-a]imidazole, and aza-(5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene).

In some embodiments, the host may be selected from the HOST Group consisting of:

and combinations thereof.

In some embodiments, the organic layer may further comprise a host, wherein the host comprises a metal complex.

In some embodiments, the compound as described herein may be a sensitizer; wherein the device may further comprise an acceptor; and wherein the acceptor may be selected from the group consisting of fluorescent emitter, delayed fluorescence emitter, and combination thereof.

In yet another aspect, the OLED of the present disclosure may also comprise an emissive region containing a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the emissive region can comprise a compound comprising a first ligand L_(A) of Formula I as defined herein.

In some embodiments, at least one of the anode, the cathode, or a new layer disposed over the organic emissive layer functions as an enhancement layer. The enhancement layer comprises a plasmonic material exhibiting surface plasmon resonance that non-radiatively couples to the emitter material and transfers excited state energy from the emitter material to non-radiative mode of surface plasmon polariton. The enhancement layer is provided no more than a threshold distance away from the organic emissive layer, wherein the emitter material has a total non-radiative decay rate constant and a total radiative decay rate constant due to the presence of the enhancement layer and the threshold distance is where the total non-radiative decay rate constant is equal to the total radiative decay rate constant. In some embodiments, the OLED further comprises an outcoupling layer. In some embodiments, the outcoupling layer is disposed over the enhancement layer on the opposite side of the organic emissive layer. In some embodiments, the outcoupling layer is disposed on opposite side of the emissive layer from the enhancement layer but still outcouples energy from the surface plasmon mode of the enhancement layer. The outcoupling layer scatters the energy from the surface plasmon polaritons. In some embodiments this energy is scattered as photons to free space. In other embodiments, the energy is scattered from the surface plasmon mode into other modes of the device such as but not limited to the organic waveguide mode, the substrate mode, or another waveguiding mode. If energy is scattered to the non-free space mode of the OLED other outcoupling schemes could be incorporated to extract that energy to free space. In some embodiments, one or more intervening layer can be disposed between the enhancement layer and the outcoupling layer. The examples for interventing layer(s) can be dielectric materials, including organic, inorganic, perovskites, oxides, and may include stacks and/or mixtures of these materials.

The enhancement layer modifies the effective properties of the medium in which the emitter material resides resulting in any or all of the following: a decreased rate of emission, a modification of emission line-shape, a change in emission intensity with angle, a change in the stability of the emitter material, a change in the efficiency of the OLED, and reduced efficiency roll-off of the OLED device. Placement of the enhancement layer on the cathode side, anode side, or on both sides results in OLED devices which take advantage of any of the above-mentioned effects. In addition to the specific functional layers mentioned herein and illustrated in the various OLED examples shown in the figures, the OLEDs according to the present disclosure may include any of the other functional layers often found in OLEDs.

The enhancement layer can be comprised of plasmonic materials, optically active metamaterials, or hyperbolic metamaterials. As used herein, a plasmonic material is a material in which the real part of the dielectric constant crosses zero in the visible or ultraviolet region of the electromagnetic spectrum. In some embodiments, the plasmonic material includes at least one metal. In such embodiments the metal may include at least one of Ag, Al, Au, Ir, Pt, Ni, Cu, W, Ta, Fe, Cr, Mg, Ga, Rh, Ti, Ru, Pd, In, Bi, Ca alloys or mixtures of these materials, and stacks of these materials. In general, a metamaterial is a medium composed of different materials where the medium as a whole acts differently than the sum of its material parts. In particular, we define optically active metamaterials as materials which have both negative permittivity and negative permeability. Hyperbolic metamaterials, on the other hand, are anisotropic media in which the permittivity or permeability are of different sign for different spatial directions. Optically active metamaterials and hyperbolic metamaterials are strictly distinguished from many other photonic structures such as Distributed Bragg Reflectors (“DBRs”) in that the medium should appear uniform in the direction of propagation on the length scale of the wavelength of light. Using terminology that one skilled in the art can understand: the dielectric constant of the metamaterials in the direction of propagation can be described with the effective medium approximation. Plasmonic materials and metamaterials provide methods for controlling the propagation of light that can enhance OLED performance in a number of ways.

In some embodiments, the enhancement layer is provided as a planar layer. In other embodiments, the enhancement layer has wavelength-sized features that are arranged periodically, quasi-periodically, or randomly, or sub-wavelength-sized features that are arranged periodically, quasi-periodically, or randomly. In some embodiments, the wavelength-sized features and the sub-wavelength-sized features have sharp edges.

In some embodiments, the outcoupling layer has wavelength-sized features that are arranged periodically, quasi-periodically, or randomly, or sub-wavelength-sized features that are arranged periodically, quasi-periodically, or randomly. In some embodiments, the outcoupling layer may be composed of a plurality of nanoparticles and in other embodiments the outcoupling layer is composed of a plurality of nanoparticles disposed over a material. In these embodiments the outcoupling may be tunable by at least one of varying a size of the plurality of nanoparticles, varying a shape of the plurality of nanoparticles, changing a material of the plurality of nanoparticles, adjusting a thickness of the material, changing the refractive index of the material or an additional layer disposed on the plurality of nanoparticles, varying a thickness of the enhancement layer, and/or varying the material of the enhancement layer. The plurality of nanoparticles of the device may be formed from at least one of metal, dielectric material, semiconductor materials, an alloy of metal, a mixture of dielectric materials, a stack or layering of one or more materials, and/or a core of one type of material and that is coated with a shell of a different type of material. In some embodiments, the outcoupling layer is composed of at least metal nanoparticles wherein the metal is selected from the group consisting of Ag, Al, Au, Ir, Pt, Ni, Cu, W, Ta, Fe, Cr, Mg, Ga, Rh, Ti, Ru, Pd, In, Bi, Ca, alloys or mixtures of these materials, and stacks of these materials. The plurality of nanoparticles may have additional layer disposed over them. In some embodiments, the polarization of the emission can be tuned using the outcoupling layer. Varying the dimensionality and periodicity of the outcoupling layer can select a type of polarization that is preferentially outcoupled to air. In some embodiments the outcoupling layer also acts as an electrode of the device.

In yet another aspect, the present disclosure also provides a consumer product comprising an organic light-emitting device (OLED) having an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer may comprise a compound as disclosed in the above compounds section of the present disclosure.

In some embodiments, the consumer product comprises an OLED having an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer can comprise a compound comprising a first ligand L_(A) of Formula I as defined herein.

In some embodiments, the consumer product can be one of a flat panel display, a computer monitor, a medical monitor, a television, a billboard, a light for interior or exterior illumination and/or signaling, a heads-up display, a fully or partially transparent display, a flexible display, a laser printer, a telephone, a cell phone, tablet, a phablet, a personal digital assistant (PDA), a wearable device, a laptop computer, a digital camera, a camcorder, a viewfinder, a micro-display that is less than 2 inches diagonal, a 3-D display, a virtual reality or augmented reality display, a vehicle, a video wall comprising multiple displays tiled together, a theater or stadium screen, a light therapy device, and a sign.

Generally, an OLED comprises at least one organic layer disposed between and electrically connected to an anode and a cathode. When a current is applied, the anode injects holes and the cathode injects electrons into the organic layer(s). The injected holes and electrons each migrate toward the oppositely charged electrode. When an electron and hole localize on the same molecule, an “exciton,” which is a localized electron-hole pair having an excited energy state, is formed. Light is emitted when the exciton relaxes via a photoemissive mechanism. In some cases, the exciton may be localized on an excimer or an exciplex. Non-radiative mechanisms, such as thermal relaxation, may also occur, but are generally considered undesirable.

Several OLED materials and configurations are described in U.S. Pat. Nos. 5,844,363, 6,303,238, and 5,707,745, which are incorporated herein by reference in their entirety.

The initial OLEDs used emissive molecules that emitted light from their singlet states (“fluorescence”) as disclosed, for example, in U.S. Pat. No. 4,769,292, which is incorporated by reference in its entirety. Fluorescent emission generally occurs in a time frame of less than 10 nanoseconds.

More recently, OLEDs having emissive materials that emit light from triplet states (“phosphorescence”) have been demonstrated. Baldo et al., “Highly Efficient Phosphorescent Emission from Organic Electroluminescent Devices,” Nature, vol. 395, 151-154, 1998; (“Baldo-I”) and Baldo et al., “Very high-efficiency green organic light-emitting devices based on electrophosphorescence,” Appl. Phys. Lett., vol. 75, No. 3, 4-6 (1999) (“Baldo-II”), are incorporated by reference in their entireties. Phosphorescence is described in more detail in U.S. Pat. No. 7,279,704 at cols. 5-6, which are incorporated by reference.

FIG. 1 shows an organic light emitting device 100. The figures are not necessarily drawn to scale. Device 100 may include a substrate 110, an anode 115, a hole injection layer 120, a hole transport layer 125, an electron blocking layer 130, an emissive layer 135, a hole blocking layer 140, an electron transport layer 145, an electron injection layer 150, a protective layer 155, a cathode 160, and a barrier layer 170. Cathode 160 is a compound cathode having a first conductive layer 162 and a second conductive layer 164. Device 100 may be fabricated by depositing the layers described, in order. The properties and functions of these various layers, as well as example materials, are described in more detail in U.S. Pat. No. 7,279,704 at cols. 6-10, which are incorporated by reference.

More examples for each of these layers are available. For example, a flexible and transparent substrate-anode combination is disclosed in U.S. Pat. No. 5,844,363, which is incorporated by reference in its entirety. An example of a p-doped hole transport layer is m-MTDATA doped with F₄-TCNQ at a molar ratio of 50:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. Examples of emissive and host materials are disclosed in U.S. Pat. No. 6,303,238 to Thompson et al., which is incorporated by reference in its entirety. An example of an n-doped electron transport layer is BPhen doped with Li at a molar ratio of 1:1, as disclosed in U.S. Patent Application Publication No. 2003/0230980, which is incorporated by reference in its entirety. U.S. Pat. Nos. 5,703,436 and 5,707,745, which are incorporated by reference in their entireties, disclose examples of cathodes including compound cathodes having a thin layer of metal such as Mg:Ag with an overlying transparent, electrically-conductive, sputter-deposited ITO layer. The theory and use of blocking layers is described in more detail in U.S. Pat. No. 6,097,147 and U.S. Patent Application Publication No. 2003/0230980, which are incorporated by reference in their entireties. Examples of injection layers are provided in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety. A description of protective layers may be found in U.S. Patent Application Publication No. 2004/0174116, which is incorporated by reference in its entirety.

FIG. 2 shows an inverted OLED 200. The device includes a substrate 210, a cathode 215, an emissive layer 220, a hole transport layer 225, and an anode 230. Device 200 may be fabricated by depositing the layers described, in order. Because the most common OLED configuration has a cathode disposed over the anode, and device 200 has cathode 215 disposed under anode 230, device 200 may be referred to as an “inverted” OLED. Materials similar to those described with respect to device 100 may be used in the corresponding layers of device 200. FIG. 2 provides one example of how some layers may be omitted from the structure of device 100.

The simple layered structure illustrated in FIGS. 1 and 2 is provided by way of non-limiting example, and it is understood that embodiments of the present disclosure may be used in connection with a wide variety of other structures. The specific materials and structures described are exemplary in nature, and other materials and structures may be used. Functional OLEDs may be achieved by combining the various layers described in different ways, or layers may be omitted entirely, based on design, performance, and cost factors. Other layers not specifically described may also be included. Materials other than those specifically described may be used. Although many of the examples provided herein describe various layers as comprising a single material, it is understood that combinations of materials, such as a mixture of host and dopant, or more generally a mixture, may be used. Also, the layers may have various sublayers. The names given to the various layers herein are not intended to be strictly limiting. For example, in device 200, hole transport layer 225 transports holes and injects holes into emissive layer 220, and may be described as a hole transport layer or a hole injection layer. In one embodiment, an OLED may be described as having an “organic layer” disposed between a cathode and an anode. This organic layer may comprise a single layer, or may further comprise multiple layers of different organic materials as described, for example, with respect to FIGS. 1 and 2.

Structures and materials not specifically described may also be used, such as OLEDs comprised of polymeric materials (PLEDs) such as disclosed in U.S. Pat. No. 5,247,190 to Friend et al., which is incorporated by reference in its entirety. By way of further example, OLEDs having a single organic layer may be used. OLEDs may be stacked, for example as described in U.S. Pat. No. 5,707,745 to Forrest et al, which is incorporated by reference in its entirety. The OLED structure may deviate from the simple layered structure illustrated in FIGS. 1 and 2. For example, the substrate may include an angled reflective surface to improve out-coupling, such as a mesa structure as described in U.S. Pat. No. 6,091,195 to Forrest et al., and/or a pit structure as described in U.S. Pat. No. 5,834,893 to Bulovic et al., which are incorporated by reference in their entireties.

Unless otherwise specified, any of the layers of the various embodiments may be deposited by any suitable method. For the organic layers, preferred methods include thermal evaporation, ink-jet, such as described in U.S. Pat. Nos. 6,013,982 and 6,087,196, which are incorporated by reference in their entireties, organic vapor phase deposition (OVPD), such as described in U.S. Pat. No. 6,337,102 to Forrest et al., which is incorporated by reference in its entirety, and deposition by organic vapor jet printing (OVJP), such as described in U.S. Pat. No. 7,431,968, which is incorporated by reference in its entirety. Other suitable deposition methods include spin coating and other solution based processes. Solution based processes are preferably carried out in nitrogen or an inert atmosphere. For the other layers, preferred methods include thermal evaporation. Preferred patterning methods include deposition through a mask, cold welding such as described in U.S. Pat. Nos. 6,294,398 and 6,468,819, which are incorporated by reference in their entireties, and patterning associated with some of the deposition methods such as ink-jet and organic vapor jet printing (OVJP). Other methods may also be used. The materials to be deposited may be modified to make them compatible with a particular deposition method. For example, substituents such as alkyl and aryl groups, branched or unbranched, and preferably containing at least 3 carbons, may be used in small molecules to enhance their ability to undergo solution processing. Substituents having 20 carbons or more may be used, and 3-20 carbons are a preferred range. Materials with asymmetric structures may have better solution processability than those having symmetric structures, because asymmetric materials may have a lower tendency to recrystallize. Dendrimer substituents may be used to enhance the ability of small molecules to undergo solution processing.

Devices fabricated in accordance with embodiments of the present disclosure may further optionally comprise a barrier layer. One purpose of the barrier layer is to protect the electrodes and organic layers from damaging exposure to harmful species in the environment including moisture, vapor and/or gases, etc. The barrier layer may be deposited over, under or next to a substrate, an electrode, or over any other parts of a device including an edge. The barrier layer may comprise a single layer, or multiple layers. The barrier layer may be formed by various known chemical vapor deposition techniques and may include compositions having a single phase as well as compositions having multiple phases. Any suitable material or combination of materials may be used for the barrier layer. The barrier layer may incorporate an inorganic or an organic compound or both. The preferred barrier layer comprises a mixture of a polymeric material and a non-polymeric material as described in U.S. Pat. No. 7,968,146, PCT Pat. Application Nos. PCT/US2007/023098 and PCT/US2009/042829, which are herein incorporated by reference in their entireties. To be considered a “mixture”, the aforesaid polymeric and non-polymeric materials comprising the barrier layer should be deposited under the same reaction conditions and/or at the same time. The weight ratio of polymeric to non-polymeric material may be in the range of 95:5 to 5:95. The polymeric material and the non-polymeric material may be created from the same precursor material. In one example, the mixture of a polymeric material and a non-polymeric material consists essentially of polymeric silicon and inorganic silicon.

Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of electronic component modules (or units) that can be incorporated into a variety of electronic products or intermediate components. Examples of such electronic products or intermediate components include display screens, lighting devices such as discrete light source devices or lighting panels, etc. that can be utilized by the end-user product manufacturers. Such electronic component modules can optionally include the driving electronics and/or power source(s). Devices fabricated in accordance with embodiments of the present disclosure can be incorporated into a wide variety of consumer products that have one or more of the electronic component modules (or units) incorporated therein. A consumer product comprising an OLED that includes the compound of the present disclosure in the organic layer in the OLED is disclosed. Such consumer products would include any kind of products that include one or more light source(s) and/or one or more of some type of visual displays. Some examples of such consumer products include flat panel displays, curved displays, computer monitors, medical monitors, televisions, billboards, lights for interior or exterior illumination and/or signaling, heads-up displays, fully or partially transparent displays, flexible displays, rollable displays, foldable displays, stretchable displays, laser printers, telephones, mobile phones, tablets, phablets, personal digital assistants (PDAs), wearable devices, laptop computers, digital cameras, camcorders, viewfinders, micro-displays (displays that are less than 2 inches diagonal), 3-D displays, virtual reality or augmented reality displays, vehicles, video walls comprising multiple displays tiled together, theater or stadium screen, a light therapy device, and a sign. Various control mechanisms may be used to control devices fabricated in accordance with the present disclosure, including passive matrix and active matrix. Many of the devices are intended for use in a temperature range comfortable to humans, such as 18 degrees C. to 30 degrees C., and more preferably at room temperature (20-25° C.), but could be used outside this temperature range, for example, from −40 degree C. to +80° C.

More details on OLEDs, and the definitions described above, can be found in U.S. Pat. No. 7,279,704, which is incorporated herein by reference in its entirety.

The materials and structures described herein may have applications in devices other than OLEDs. For example, other optoelectronic devices such as organic solar cells and organic photodetectors may employ the materials and structures. More generally, organic devices, such as organic transistors, may employ the materials and structures.

In some embodiments, the OLED has one or more characteristics selected from the group consisting of being flexible, being rollable, being foldable, being stretchable, and being curved. In some embodiments, the OLED is transparent or semi-transparent. In some embodiments, the OLED further comprises a layer comprising carbon nanotubes.

In some embodiments, the OLED further comprises a layer comprising a delayed fluorescent emitter. In some embodiments, the OLED comprises a RGB pixel arrangement or white plus color filter pixel arrangement. In some embodiments, the OLED is a mobile device, a hand held device, or a wearable device. In some embodiments, the OLED is a display panel having less than 10 inch diagonal or 50 square inch area. In some embodiments, the OLED is a display panel having at least 10 inch diagonal or 50 square inch area. In some embodiments, the OLED is a lighting panel.

In some embodiments, the compound can be an emissive dopant. In some embodiments, the compound can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence; see, e.g., U.S. application Ser. No. 15/700,352, which is hereby incorporated by reference in its entirety), triplet-triplet annihilation, or combinations of these processes. In some embodiments, the emissive dopant can be a racemic mixture, or can be enriched in one enantiomer. In some embodiments, the compound can be homoleptic (each ligand is the same). In some embodiments, the compound can be heteroleptic (at least one ligand is different from others). When there are more than one ligand coordinated to a metal, the ligands can all be the same in some embodiments. In some other embodiments, at least one ligand is different from the other ligands. In some embodiments, every ligand can be different from each other. This is also true in embodiments where a ligand being coordinated to a metal can be linked with other ligands being coordinated to that metal to form a tridentate, tetradentate, pentadentate, or hexadentate ligands. Thus, where the coordinating ligands are being linked together, all of the ligands can be the same in some embodiments, and at least one of the ligands being linked can be different from the other ligand(s) in some other embodiments.

In some embodiments, the compound can be used as a phosphorescent sensitizer in an OLED where one or multiple layers in the OLED contains an acceptor in the form of one or more fluorescent and/or delayed fluorescence emitters. In some embodiments, the compound can be used as one component of an exciplex to be used as a sensitizer. As a phosphorescent sensitizer, the compound must be capable of energy transfer to the acceptor and the acceptor will emit the energy or further transfer energy to a final emitter. The acceptor concentrations can range from 0.001% to 100%. The acceptor could be in either the same layer as the phosphorescent sensitizer or in one or more different layers. In some embodiments, the acceptor is a TADF emitter. In some embodiments, the acceptor is a fluorescent emitter. In some embodiments, the emission can arise from any or all of the sensitizer, acceptor, and final emitter

According to another aspect, a formulation comprising the compound described herein is also disclosed.

The OLED disclosed herein can be incorporated into one or more of a consumer product, an electronic component module, and a lighting panel. The organic layer can be an emissive layer and the compound can be an emissive dopant in some embodiments, while the compound can be a non-emissive dopant in other embodiments.

In yet another aspect of the present disclosure, a formulation that comprises the novel compound disclosed herein is described. The formulation can include one or more components selected from the group consisting of a solvent, a host, a hole injection material, hole transport material, electron blocking material, hole blocking material, and an electron transport material, disclosed herein.

The present disclosure encompasses any chemical structure comprising the novel compound of the present disclosure, or a monovalent or polyvalent variant thereof. In other words, the inventive compound, or a monovalent or polyvalent variant thereof, can be a part of a larger chemical structure. Such chemical structure can be selected from the group consisting of a monomer, a polymer, a macromolecule, and a supramolecule (also known as supermolecule). As used herein, a “monovalent variant of a compound” refers to a moiety that is identical to the compound except that one hydrogen has been removed and replaced with a bond to the rest of the chemical structure. As used herein, a “polyvalent variant of a compound” refers to a moiety that is identical to the compound except that more than one hydrogen has been removed and replaced with a bond or bonds to the rest of the chemical structure. In the instance of a supramolecule, the inventive compound can also be incorporated into the supramolecule complex without covalent bonds.

D. Combination of the Compounds of the Present Disclosure with Other Materials

The materials described herein as useful for a particular layer in an organic light emitting device may be used in combination with a wide variety of other materials present in the device. For example, emissive dopants disclosed herein may be used in conjunction with a wide variety of hosts, transport layers, blocking layers, injection layers, electrodes and other layers that may be present. The materials described or referred to below are non-limiting examples of materials that may be useful in combination with the compounds disclosed herein, and one of skill in the art can readily consult the literature to identify other materials that may be useful in combination.

a) Conductivity Dopants:

A charge transport layer can be doped with conductivity dopants to substantially alter its density of charge carriers, which will in turn alter its conductivity. The conductivity is increased by generating charge carriers in the matrix material, and depending on the type of dopant, a change in the Fermi level of the semiconductor may also be achieved. Hole-transporting layer can be doped by p-type conductivity dopants and n-type conductivity dopants are used in the electron-transporting layer.

Non-limiting examples of the conductivity dopants that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP01617493, EP01968131, EP2020694, EP2684932, US20050139810, US20070160905, US20090167167, US2010288362, WO06081780, WO2009003455, WO2009008277, WO2009011327, WO2014009310, US2007252140, US2015060804, US20150123047, and US2012146012.

b) HIL/HTL:

A hole injecting/transporting material to be used in the present disclosure is not particularly limited, and any compound may be used as long as the compound is typically used as a hole injecting/transporting material. Examples of the material include, but are not limited to: a phthalocyanine or porphyrin derivative; an aromatic amine derivative; an indolocarbazole derivative; a polymer containing fluorohydrocarbon; a polymer with conductivity dopants; a conducting polymer, such as PEDOT/PSS; a self-assembly monomer derived from compounds such as phosphonic acid and silane derivatives; a metal oxide derivative, such as MoO_(x); a p-type semiconducting organic compound, such as 1,4,5,8,9,12-Hexaazatriphenylenehexacarbonitrile; a metal complex, and a cross-linkable compounds.

Examples of aromatic amine derivatives used in HIL or HTL include, but not limit to the following general structures:

Each of Ar¹ to Ar⁹ is selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each Ar may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, Ar¹ to Ar⁹ is independently selected from the group consisting of:

wherein k is an integer from 1 to 20; X¹⁰¹ to X¹⁰⁸ is C (including CH) or N; Z¹⁰¹ is NAr¹, O, or S; Ar¹ has the same group defined above.

Examples of metal complexes used in HIL or HTL include, but are not limited to the following general formula:

wherein Met is a metal, which can have an atomic weight greater than 40; (Y¹⁰¹-Y¹⁰²) is a bidentate ligand, Y¹⁰¹ and Y¹⁰² are independently selected from C, N, O, P, and S; L¹⁰¹ is an ancillary ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, (Y¹⁰¹-Y¹⁰²) is a 2-phenylpyridine derivative. In another aspect, (Y¹⁰¹-Y¹⁰²) is a carbene ligand. In another aspect, Met is selected from Ir, Pt, Os, and Zn. In a further aspect, the metal complex has a smallest oxidation potential in solution vs. Fc⁺/Fc couple less than about 0.6 V.

Non-limiting examples of the HIL and HTL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN102702075, DE102012005215, EP01624500, EP01698613, EP01806334, EP01930964, EP01972613, EP01997799, EP02011790, EP02055700, EP02055701, EP1725079, EP2085382, EP2660300, EP650955, JP07-073529, JP2005112765, JP2007091719, JP2008021687, JP2014-009196, KR20110088898, KR20130077473, TW201139402, U.S. Ser. No. 06/517,957, US20020158242, US20030162053, US20050123751, US20060182993, US20060240279, US20070145888, US20070181874, US20070278938, US20080014464, US20080091025, US20080106190, US20080124572, US20080145707, US20080220265, US20080233434, US20080303417, US2008107919, US20090115320, US20090167161, US2009066235, US2011007385, US20110163302, US2011240968, US2011278551, US2012205642, US2013241401, US20140117329, US2014183517, U.S. Pat. Nos. 5,061,569, 5,639,914, WO05075451, WO07125714, WO08023550, WO08023759, WO2009145016, WO2010061824, WO2011075644, WO2012177006, WO2013018530, WO2013039073, WO2013087142, WO2013118812, WO2013120577, WO2013157367, WO2013175747, WO2014002873, WO2014015935, WO2014015937, WO2014030872, WO2014030921, WO2014034791, WO2014104514, WO2014157018.

c) EBL:

An electron blocking layer (EBL) may be used to reduce the number of electrons and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies, and/or longer lifetime, as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than the emitter closest to the EBL interface. In some embodiments, the EBL material has a higher LUMO (closer to the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the EBL interface. In one aspect, the compound used in EBL contains the same molecule or the same functional groups used as one of the hosts described below.

d) Hosts:

The light emitting layer of the organic EL device of the present disclosure preferably contains at least a metal complex as light emitting material, and may contain a host material using the metal complex as a dopant material. Examples of the host material are not particularly limited, and any metal complexes or organic compounds may be used as long as the triplet energy of the host is larger than that of the dopant. Any host material may be used with any dopant so long as the triplet criteria is satisfied.

Examples of metal complexes used as host are preferred to have the following general formula:

wherein Met is a metal; (Y¹⁰³-Y¹⁰⁴) is a bidentate ligand, Y¹⁰³ and Y¹⁰⁴ are independently selected from C, N, O, P, and S; L¹⁰¹ is an another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal; and k′+k″ is the maximum number of ligands that may be attached to the metal.

In one aspect, the metal complexes are:

wherein (O—N) is a bidentate ligand, having metal coordinated to atoms O and N.

In another aspect, Met is selected from Ir and Pt. In a further aspect, (Y¹⁰³-Y¹⁰⁴) is a carbene ligand.

In one aspect, the host compound contains at least one of the following groups selected from the group consisting of aromatic hydrocarbon cyclic compounds such as benzene, biphenyl, triphenyl, triphenylene, tetraphenylene, naphthalene, anthracene, phenalene, phenanthrene, fluorene, pyrene, chrysene, perylene, and azulene; the group consisting of aromatic heterocyclic compounds such as dibenzothiophene, dibenzofuran, dibenzoselenophene, furan, thiophene, benzofuran, benzothiophene, benzoselenophene, carbazole, indolocarbazole, pyridylindole, pyrrolodipyridine, pyrazole, imidazole, triazole, oxazole, thiazole, oxadiazole, oxatriazole, dioxazole, thiadiazole, pyridine, pyridazine, pyrimidine, pyrazine, triazine, oxazine, oxathiazine, oxadiazine, indole, benzimidazole, indazole, indoxazine, benzoxazole, benzisoxazole, benzothiazole, quinoline, isoquinoline, cinnoline, quinazoline, quinoxaline, naphthyridine, phthalazine, pteridine, xanthene, acridine, phenazine, phenothiazine, phenoxazine, benzofuropyridine, furodipyridine, benzothienopyridine, thienodipyridine, benzoselenophenopyridine, and selenophenodipyridine; and the group consisting of 2 to 10 cyclic structural units which are groups of the same type or different types selected from the aromatic hydrocarbon cyclic group and the aromatic heterocyclic group and are bonded to each other directly or via at least one of oxygen atom, nitrogen atom, sulfur atom, silicon atom, phosphorus atom, boron atom, chain structural unit and the aliphatic cyclic group. Each option within each group may be unsubstituted or may be substituted by a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.

In one aspect, the host compound contains at least one of the following groups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, and when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. k is an integer from 0 to 20 or 1 to 20. X¹⁰¹ to X¹⁰⁸ are independently selected from C (including CH) or N. Z¹⁰¹ and Z¹⁰² are independently selected from NR¹⁰¹, O, or S.

Non-limiting examples of the host materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: EP2034538, EP2034538A, EP2757608, JP2007254297, KR20100079458, KR20120088644, KR20120129733, KR20130115564, TW201329200, US20030175553, US20050238919, US20060280965, US20090017330, US20090030202, US20090167162, US20090302743, US20090309488, US20100012931, US20100084966, US20100187984, US2010187984, US2012075273, US2012126221, US2013009543, US2013105787, US2013175519, US2014001446, US20140183503, US20140225088, US2014034914, U.S. Pat. No. 7,154,114, WO2001039234, WO2004093207, WO2005014551, WO2005089025, WO2006072002, WO2006114966, WO2007063754, WO2008056746, WO2009003898, WO2009021126, WO2009063833, WO2009066778, WO2009066779, WO2009086028, WO2010056066, WO2010107244, WO2011081423, WO2011081431, WO2011086863, WO2012128298, WO2012133644, WO2012133649, WO2013024872, WO2013035275, WO2013081315, WO2013191404, WO2014142472, US20170263869, US20160163995, U.S. Pat. No. 9,466,803,

e) Additional Emitters:

One or more additional emitter dopants may be used in conjunction with the compound of the present disclosure. Examples of the additional emitter dopants are not particularly limited, and any compounds may be used as long as the compounds are typically used as emitter materials. Examples of suitable emitter materials include, but are not limited to, compounds which can produce emissions via phosphorescence, fluorescence, thermally activated delayed fluorescence, i.e., TADF (also referred to as E-type delayed fluorescence), triplet-triplet annihilation, or combinations of these processes. Non-limiting examples of the emitter materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103694277, CN1696137, EB01238981, EP01239526, EP01961743, EP1239526, EP1244155, EP1642951, EP1647554, EP1841834, EP1841834B, EP2062907, EP2730583, JP2012074444, JP2013110263, JP4478555, KR1020090133652, KR20120032054, KR20130043460, TW201332980, U.S. Ser. No. 06/699,599, U.S. Ser. No. 06/916,554, US20010019782, US20020034656, US20030068526, US20030072964, US20030138657, US20050123788, US20050244673, US2005123791, US2005260449, US20060008670, US20060065890, US20060127696, US20060134459, US20060134462, US20060202194, US20060251923, US20070034863, US20070087321, US20070103060, US20070111026, US20070190359, US20070231600, US2007034863, US2007104979, US2007104980, US2007138437, US2007224450, US2007278936, US20080020237, US20080233410, US20080261076, US20080297033, US200805851, US2008161567, US2008210930, US20090039776, US20090108737, US20090115322, US20090179555, US2009085476, US2009104472, US20100090591, US20100148663, US20100244004, US20100295032, US2010102716, US2010105902, US2010244004, US2010270916, US20110057559, US20110108822, US20110204333, US2011215710, US2011227049, US2011285275, US2012292601, US20130146848, US2013033172, US2013165653, US2013181190, US2013334521, US20140246656, US2014103305, U.S. Pat. Nos. 6,303,238, 6,413,656, 6,653,654, 6,670,645, 6,687,266, 6,835,469, 6,921,915, 7,279,704, 7,332,232, 7,378,162, 7,534,505, 7,675,228, 7,728,137, 7,740,957, 7,759,489, 7,951,947, 8,067,099, 8,592,586, 8,871,361, WO06081973, WO06121811, WO07018067, WO07108362, WO07115970, WO07115981, WO08035571, WO2002015645, WO2003040257, WO2005019373, WO2006056418, WO2008054584, WO2008078800, WO2008096609, WO2008101842, WO2009000673, WO2009050281, WO2009100991, WO2010028151, WO2010054731, WO2010086089, WO2010118029, WO2011044988, WO2011051404, WO2011107491, WO2012020327, WO2012163471, WO2013094620, WO2013107487, WO2013174471, WO2014007565, WO2014008982, WO2014023377, WO2014024131, WO2014031977, WO2014038456, WO2014112450.

f) HBL:

A hole blocking layer (HBL) may be used to reduce the number of holes and/or excitons that leave the emissive layer. The presence of such a blocking layer in a device may result in substantially higher efficiencies and/or longer lifetime as compared to a similar device lacking a blocking layer. Also, a blocking layer may be used to confine emission to a desired region of an OLED. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and/or higher triplet energy than the emitter closest to the HBL interface. In some embodiments, the HBL material has a lower HOMO (further from the vacuum level) and/or higher triplet energy than one or more of the hosts closest to the HBL interface.

In one aspect, compound used in HBL contains the same molecule or the same functional groups used as host described above.

In another aspect, compound used in HBL contains at least one of the following groups in the molecule:

wherein k is an integer from 1 to 20; L¹⁰¹ is another ligand, k′ is an integer from 1 to 3.

g) ETL:

Electron transport layer (ETL) may include a material capable of transporting electrons. Electron transport layer may be intrinsic (undoped), or doped. Doping may be used to enhance conductivity. Examples of the ETL material are not particularly limited, and any metal complexes or organic compounds may be used as long as they are typically used to transport electrons.

In one aspect, compound used in ETL contains at least one of the following groups in the molecule:

wherein R¹⁰¹ is selected from the group consisting of hydrogen, deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acids, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof, when it is aryl or heteroaryl, it has the similar definition as Ar's mentioned above. Ar¹ to Ar³ has the similar definition as Ar's mentioned above. k is an integer from 1 to 20. X¹⁰¹ to X¹⁰⁸ is selected from C (including CH) or N.

In another aspect, the metal complexes used in ETL contains, but not limit to the following general formula:

wherein (O—N) or (N—N) is a bidentate ligand, having metal coordinated to atoms O, N or N, N; L¹⁰¹ is another ligand; k′ is an integer value from 1 to the maximum number of ligands that may be attached to the metal.

Non-limiting examples of the ETL materials that may be used in an OLED in combination with materials disclosed herein are exemplified below together with references that disclose those materials: CN103508940, EP01602648, EP01734038, EP01956007, JP2004-022334, JP2005149918, JP2005-268199, KR0117693, KR20130108183, US20040036077, US20070104977, US2007018155, US20090101870, US20090115316, US20090140637, US20090179554, US2009218940, US2010108990, US2011156017, US2011210320, US2012193612, US2012214993, US2014014925, US2014014927, US20140284580, U.S. Pat. Nos. 6,656,612, 8,415,031, WO2003060956, WO2007111263, WO2009148269, WO2010067894, WO2010072300, WO2011074770, WO2011105373, WO2013079217, WO2013145667, WO2013180376, WO2014104499, WO2014104535,

h) Charge Generation Layer (CGL)

In tandem or stacked OLEDs, the CGL plays an essential role in the performance, which is composed of an n-doped layer and a p-doped layer for injection of electrons and holes, respectively. Electrons and holes are supplied from the CGL and electrodes. The consumed electrons and holes in the CGL are refilled by the electrons and holes injected from the cathode and anode, respectively; then, the bipolar currents reach a steady state gradually. Typical CGL materials include n and p conductivity dopants used in the transport layers.

In any above-mentioned compounds used in each layer of the OLED device, the hydrogen atoms can be partially or fully deuterated. The minimum amount of hydrogen of the compound being deuterated is selected from the group consisting of 30%, 40%, 50%, 60%, 70%, 80%, 90%, 95%, 99%, and 100%. Thus, any specifically listed substituent, such as, without limitation, methyl, phenyl, pyridyl, etc. may be undeuterated, partially deuterated, and fully deuterated versions thereof. Similarly, classes of substituents such as, without limitation, alkyl, aryl, cycloalkyl, heteroaryl, etc. also may be undeuterated, partially deuterated, and fully deuterated versions thereof.

It is understood that the various embodiments described herein are by way of example only and are not intended to limit the scope of the invention. For example, many of the materials and structures described herein may be substituted with other materials and structures without deviating from the spirit of the invention. The present invention as claimed may therefore include variations from the particular examples and preferred embodiments described herein, as will be apparent to one of skill in the art. It is understood that various theories as to why the invention works are not intended to be limiting.

E. Experimental Data

7-Chlorothieno[2,3-c]pyridine (13 g, 77 mmol), (3,5-dimethylphenyl)boronic acid (12.64 g, 84 mmol) and cesium carbonate (62.4 g, 192 mmol) were dissolved in 1,4-dioxane (250 mL) and water (62.5 mL). The solution was de-oxygenated for 10 min by bubbling nitrogen through the solution. Tetrakis(triphenylphosphine)palladium(0) (3.54 g, 3.07 mmol) was added and the reaction was heated at 110° C. for 2 hours under nitrogen. After the completion, the solution was cooled and the solvent was removed. The crude was purified to yield a pale yellow solid of 7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (18 g, 75 mmol, 98% yield).

7-(3,5-Dimethylphenyl)thieno[2,3-c]pyridine (17.8 g, 74.4 mmol) was dissolved in dry THF (250 mL). The reaction was cooled to −78° C. under nitrogen. n-Butyllithium (2.2M in hexanes) (37.2 mL, 82 mmol) was added and the reaction was stirred at this temperature for 10 min. A suspension of N-bromosuccinimide (14.56 g, 82 mmol) in THF (50 mL) was added slowly and the reaction was warmed to room temperature (RT) after 30 min at −78° C. This was then diluted with DCM (600 mL) and washed with sat. NaHCO₃ (600 mL). The aqueous layer was washed with DCM (600 mL). The combined organic layers were dried (MgSO₄) and evaporated to yield a brown oil and used as crude.

2-Bromo-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (15.94 g, 50.1 mmol), (4-chloro-2-formylphenyl)boronic acid (10.16 g, 55.1 mmol) and potassium carbonate (17.31 g, 125 mmol) were dissolved in 1,4-dioxane (250 mL) and water (50 mL). The reaction was placed under vacuum and filled back with nitrogen (3×). Tetrakis(triphenylphosphine)palladium(0) (2.89 g, 2.505 mmol) was added and the reaction heated at 70° C. under nitrogen for overnight. Additional Tetrakis(triphenylphosphine)palladium(0) (2.89 g, 2.505 mmol) was added and the reaction left stirred under nitrogen at 70° C. overnight. The reaction was cooled to RT and the solvent was evaporated. The crude was purified to yield 5-chloro-2-(7-(3,5-dimethylphenyl)thieno[2,3-c]pyridin-2-yl)benzaldehyde (12.7 g, 33.6 mmol, 67% yield over 2 steps) as a pale yellow solid.

5-Chloro-2-(7-(3,5-dimethylphenyl)thieno[2,3-c]pyridin-2-yl)benzaldehyde (12.7 g, 33.6 mmol) and (methoxymethyl)triphenylphosphonium chloride (19.59 g, 57.1 mmol) were dispersed in dry THF (200 mL). The reaction was cooled to 0° C. and after 5 min potassium 2-methylpropan-2-olate (6.41 g, 57.1 mmol) in 100 mL of dry THF was added. The reaction was stirred under nitrogen and slowly warmed to RT over 3 hours. Water was added (250 mL) and the crude was extracted with EtOAc (3×250 mL). The combined organic layers were dried (MgSO₄) and evaporated. The product was purified to yield the two isomers of 2-(4-chloro-2-(2-methoxyvinyl)phenyl)-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (9.5 g, 23.40 mmol, 69.6% yield) as a pale yellow gum.

2-(4-Chloro-2-(2-methoxyvinyl)phenyl)-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (9.2 g, 22.66 mmol) was dissolved in DCM. Methanesulfonic acid (5.88 mL, 91 mmol) was added and the reaction was stirred at RT overnight. The reaction was diluted with DCM (200 mL) and the organic layer was washed with 2M Na₂CO₃ (aq, 300 mL). The aqueous layer was extracted with DCM (3×200 mL). The combined organic layers were dried (MgSO4) and evaporated to yield a pale yellow solid of 3-chloro-10-(3,5-dimethylphenyl)naphtho[2′,1′:4,5]thieno[2,3-c]pyridine (7.5 g, 20.06 mmol, 89% yield). This was used as the crude in the next step.

Crude 3-chloro-10-(3,5-dimethylphenyl)naphtho[2′,1′:4,5]thieno[2,3-c]pyridine (7.8 g, 20.86 mmol), palladium(II) acetate (0.234 g, 1.043 mmol) and XPhos (1.082 g, 2.086 mmol) were placed in a round bottom flask (RBF) and the flask was sparged with nitrogen for 30 min. Neopentylzinc(II) iodide (0.5M in THF, 77 ml, 38.6 mmol) was added and the reaction was heated at 70° C. overnight under nitrogen. The reaction was cooled to RT and the product purified to yield the product 10-(3,5-dimethylphenyl)-3-neopentylnaphtho[2′,1′:4,5]thieno[2,3-c]pyridine (3.9 g, 9.49 mmol, 46% yield) as a colourless solid.

A mixture of 10-(3,5-dimethylphenyl)-3-neopentylnaphtho[2′,1′:4,5]thieno[2,3-c]pyridine (1.3 g, 3.16 mmol, 2.0 equiv) in 2-ethoxyethanol (12 mL) and DIUF water (3 mL) was sparged with nitrogen for 10 minutes. Iridium(III) chloride hydrate (0.50 g, 1.58 mmol, 1.0 equiv) was added and sparging continued for 5 minutes. The reaction mixture was heated at 100° C. for 20 hours. The reaction mixture was cooled to RT and filtered. The solid was washed with water (5 mL) and methanol (3×2 mL) and used as the crude in the next step reaction. To a suspension of crude in methanol (10 mL) and dichloro-methane (2 mL) were added 3,7-diethyl-nonane-4,6-dione (0.67 g, 3.16 mmol, 4.0 equiv) and powdered potassium carbonate (0.66 g, 4.74 mmol, 6.0 equiv). The reaction mixture was heated at 50° C. for 3 hours. Water (5 mL) was added to the cooled reaction mixture. The suspension was filtered and the solid washed with water (2×3 mL) and methanol (3×1 mL). The crude material was purified to give product (0.9 g, 47% yield) as an orange solid.

To a 250 mL 3-neck RBF equipped with a thermowell controller, reflux condenser, and a magnetic stir-bar was weighed 7-(3,5-dimethylphenyl)-2-iodo-4-(trifluoromethyl)thieno[2,3-c]pyridine (6.5 g, 15 mmol), dicyclohexyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphane (0.715 g, 1.5 mmol), and potassium phosphate (9.55 g, 45 mmol). the solid reagents were suspended with a solution of 2-(2-(2-methoxyvinyl)-4-neopentylphenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane (10.21 g, 30.9 mmol) in toluene (70 mL) and water (13.89 mL). The mixture was degassed with a nitrogen for 10 minutes with stirring, then Pd₂(dba)₃ (0.343 g, 0.375 mmol) was added to the reaction mixture and degassing continued for an additional 10 minutes. The reaction mixture was heated to a gentle reflux (87° C.) for 18 hours. The reaction mixture was diluted with water (100 mL) and DCM (200 mL) and the organic layer was separated, the aqueous layer was extracted with DCM (3×70 mL). The combined organic extracts were dried over Na₂SO₄, filtered, and concentrated to dryness. The crude residue was purified by chromatography on silica gel eluting with DCM:Heptane using a gradient of 5 to 40% to give a yellow oil (2.56 g, 4.79 mmol, 31.9% yield).

To a 250 mL RBF equipped with a magnetic stir-bar and metal thermocouple needle insert under nitrogen atmosphere, a solution 7-(3,5-dimethylphenyl)-2-(2-(2-methoxyvinyl)-4-neopentylphenyl)-4-(trifluoromethyl)thieno[2,3-c]pyridine (2.6 g, 5.10 mmol) was prepared in DCM (43 mL). The reaction mixture was cooled to 0° C. with an ice-bath, MsOH with 7.7 wt % P₂O₅ (4.21 mL, 26.5 mmol) was added slowly over 10 minutes by syringe. The reaction mixture was stirred for 18 hours while warming to RT. The reaction mixture was poured into water (200 mL) and stirred for 20 minutes. The organic layer was separated from the biphasic mixture, and the aqueous phase was extracted with DCM (3×50 mL). The combined organic extracts were dried over Na₂SO₄, filtered, and concentrated to dryness. The crude yellow solid was dissolved in hot DCM (20 mL) and poured into MeOH (150 mL) and stirred for 2 hours. The light yellow solid was isolated by buchner funnel filtration and washed with methanol (50 mL) to give white solid (1.098 g).

A solution of 10-(3,5-dimethylphenyl)-3-neopentyl-7-(trifluoromethyl)naphtho[2′,1′:4,5]thieno[2,3-c]pyridine (0.77 g, 1.61 mmol) and Iridium(III) chloride hydrate (0.27 g, 0.77 mmol) was sparging for 5 minutes. The reaction mixture was heated at 130° C. for 20 hours. The reaction mixture was cooled to RT. To the suspension were added 3,7-diethyl-nonane-4,6-dione (0.45 g, 2.10 mmol) and powdered potassium carbonate (0.29 g, 2.10 mmol). The reaction mixture was heated at 50° C. for 24 hours. The crude material was purified to give product (0.5 g, 48%).

To a 1 L flask under nitrogen was added 7-(3,5-dimethylphenyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thieno[2,3-c]pyridine (20.0 g, 54.7 mmol), 2-chloro-4,6-difluorobenzaldehyde (10.63 g, 60.2 mmol), potassium phosphate (34.9 g, 164 mmol), dicyclohexyl(2′,4′,6′-triisopropyl-[1,1′-biphenyl]-2-yl)phosphane (3.13 g, 6.57 mmol), Pd₂(dba)₃ (3.01 g, 3.28 mmol), toluene (277 mL), and water (27.7 mL). The mixture was stirred and heated to reflux (90° C.) overnight. After 16 hours, the reaction mixture was cooled to RT, diluted with water (500 mL) and the organic layer was separated. The aqueous layer was extracted with DCM (3×500 mL) and the combined organic layers were dried over Na₂SO₄, filtered, and concentrated. The orange solid was dissolved in DCM and passed through a silica gel (800 g) plug. The plug was washed with EtOAc/heptane (0%-40%) and EtOAc/DCM (10%). Concentration of the fractions followed by the heptane (1 L) trituration gave 2-(7-(3,5-dimethylphenyl)thieno[2,3-c]pyridin-2-yl)-4,6-difluorobenzaldehyde (16.2 g, 78% yield) as a light yellow solid.

(Methoxymethyl)triphenylphosphonium chloride (22.01 g, 64.2 mmol) and THF (350 mL) were added to a 1 L flask under nitrogen. The resulting solution was cooled to 0° C. and potassium tert-butoxide (7.20 g, 64.2 mmol) was added. The mixture turned red and was stirred at RT for 1 hour. Then the solution was cooled to 0° C. and a solution of 2-(7-(3,5-dimethylphenyl)thieno[2,3-c]pyridin-2-yl)-4,6-difluorobenzaldehyde (16.24 g, 42.8 mmol) in THF (300 mL) was added. The resulting mixture was stirred at 0° C. for 1 hour and at RT for 2 hour. The reaction mixture was quenched with water (400 mL) and extracted with DCM (3×400 mL). The combined organic layer was dried over Na₂SO₄, filtered, and concentrated. The yellow solid was dissolved in DCM (0.5 L), filtered through a plug of silica gel (300 g) and plug was eluted with DCM. The fractions containing product were combined and concentrated to give 2-(3,5-difluoro-2-(2-methoxyvinyl)phenyl)-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (15.71 g, 90%, 8:2 trans/cis ratio) as an off-white solid.

Under nitrogen was added 2-(3,5-difluoro-2-(2-methoxyvinyl)phenyl)-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (15.65 g, 38.4 mmol) (80% trans and 20% cis) in dichloromethane (312 mL). The resulting mixture was stirred, and to this mixture was added Eaton's Reagent (31.3 mL, 197 mmol) slowly over 10 min. After being stirred for 20 hours at RT, the reaction mixture was poured into the water (3.5 L). The resulting solid was collected via suction filtration, washed with water and triturated with MeOH (300 mL) to give an off-white solid. The solid (˜9.5 g) was suspended in DCM and filtered through a plug of silica gel (300 g) and plug was eluted with EtOAc/DCM (0%-10%). The fractions containing product were concentrated and the resulting solid was triturated with EtOAc followed by DCM to afford 10-(3,5-dimethylphenyl)-2,4-difluoronaphtho[2′,1′:4,5]thieno[2,3-c]pyridine (7.28 g, 50% yield) as a white solid.

A suspended mixture of 10-(3,5-dimethylphenyl)-2,4-difluoronaphtho [2′,1′:4,5]thieno[2,3-c]pyridine (4.15 g, 11.05 mmol, 2.2 equiv) and iridium(III) chloride hydrate (1.5 g, 5.02 mmol, 1.0 equiv) in 2-ethoxyethanol (45 mL) and deionized ultra-filtered (DIUF) water (15 mL) was heated at 100° C. overnight. The reaction mixture was cooled to RT and diluted with DIUF water (25 mL). The red solid was filtered and washed with methanol (10 mL). To the mixture (est. 2.51 mmol, 1.0 equiv) in dichloromethane (25 mL) and methanol (25 mL) were added 3,7-diethylnonane-4,6-dione (1.07 g, 5.03 mmol, 2.0 equiv) and powdered potassium carbonate (1.04 g, 7.54 mmol, 3.0 equiv). The mixture was heated at 42° C. overnight. The reaction mixture was cooled to RT, DIUF water (100 mL) was added and the suspension filtered. The red solid was purified to give product (1.28 g, 22% yield) as a bright red solid.

A mixture of 7-(3,5-dimethylphenyl)-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)thieno[2,3-c]pyridine (6.0 g, 14.78 mmol), 1-bromo-2-(2,2-dimethoxyethyl)-3,5-bis(trifluoromethyl)benzene (7.32 g, 19.22 mmol) and tripotassium phosphate (9.41 g, 44.3 mmol) in toluene (70 mL) was degassed by bubbling with N₂ for 10 min, then XPhosPdG4 (0.636 g, 0.739 mmol) and XPhos (0.352 g, 0.739 mmol) was added. The mixture was stirred at 80° C. for 4 days, cooled to RT, diluted with DCM (100 mL), filtered through Celite (diatomaceous earth) and concentrated onto silica to give 2-(2-(2,2-dimethoxyethyl)-3,5-bis(trifluoromethyl)phenyl)-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (4.84 g, 8.52 mmol, 57.7% yield) as a pale yellow oil.

Methanesulfonic acid (5.5 mL, 85 mmol) was added to a solution of 2-(2-(2,2-dimethoxyethyl)-3,5-bis(trifluoromethyl)phenyl)-7-(3,5-dimethylphenyl)thieno[2,3-c]pyridine (4.84 g, 8.52 mmol) in DCM (40 mL). The mixture was stirred at RT for 22 hours, diluted with 2 M NaOH (200 mL) and extracted with DCM (3×70 mL). The combined organic phases were dried (Na2SO4), filtered and concentrated onto Celite to give 10-(3,5-dimethylphenyl)-2,4-bis(trifluoromethyl)naphtho[2′,1′:4,5]thieno[2,3-c]pyridine (3.01 g, 6.33 mmol, 74.3% yield) as a colourless solid.

A solution of 10-(3,5-dimethylphenyl)-2,4-bis(trifluoromethyl)naphtho[2′,1′:4,5]thieno[2,3-c]pyridine (1.48 g, 3.12 mmol) and Iridium(III) chloride hydrate (0.55 g, 1.56 mmol) was sparging for 5 minutes. The reaction mixture was heated at 130° C. for 20 hours. The reaction mixture was cooled to RT. 3,7-diethyl-nonane-4,6-dione (0.98 g, 4.59 mmol) and powdered potassium carbonate (0.63 g, 4.59 mmol) were added to the suspension. The reaction mixture was heated at 50° C. for 24 hours. The crude material was purified to product (0.53 g, 26%).

Methyl iodide (16.74 mL, 269 mmol) was added dropwise to a solution of 7-bromonaphthalen-2-ol (40 g, 179 mmol) and potassium carbonate (49.6 g, 359 mmol) in DMF (543 mL) and the reaction mixture was stirred overnight at RT. The reaction mixture was separated between TBME (800 mL) and sat. aq. NH₄Cl (500 mL) then washed with sat. aq. NH₄Cl (3×400 ml) followed by brine (400 mL). The organics were dried over MgSO₄, filtered and concentrated in vacuo to give 2-bromo-7-methoxynaphthalene as a light beige solid (41.5 g, 95%).

Magnesium turnings (5.17 g, 213 mmol) and one crystal of iodide were placed in the flask and then it was placed under nitrogen. THF (400 mL) was added to a dropping funnel and a small amount of THF was added to the flask to cover the magnesium turnings. 1-bromo-2,2-dimethylpropane (20.85 mL, 166 mmol) was added to the THF in the dropping funnel. A quarter of this solution was added to the magnesium and the Grignard formation initiated by heating with a heat gun (to reflux). The rest of the bromide solution was added dropwise at RT over 15 minutes then the mixture was stirred for 1 hour. The mixture turned a dark-orange-brown colour and most of the magnesium was consumed. 2-bromo-7-methoxynaphthalene (14 g, 59.0 mmol), palladium acetate (0.663 g, 2.95 mmol) and XPhos (2.111 g, 4.43 mmol) were added to an RBF and the flask was placed under nitrogen. 100 mL of dry THF was added to the solution in the RBF and the solution was cooled to 0° C. (ice/water). The Grignard solution was transferred via cannula over 30 min and the reaction mixture stirred at RT for 30 minutes. The reaction mixture was quenched by addition of water (5 mL) and concentrated in vacuo to give a dark oily residue. The dark oily residue was filtered through a silica plug (350 g silica plus 50 g of dicalite) eluting with 5% EtOAc in heptane (2 L) then 10% EtOAc (1 L) to give 2-methoxy-7-neopentylnaphthalene as a yellow solid (39.2 g, 97%).

A solution of 2-methoxy-7-neopentylnaphthalene (20 g, 88 mmol) in tetrahydrofuran (300 mL) was cooled to −78° C. (dry-ice/acetone) then n-butyllithium (2.1M in hexanes) (45.7 mL, 105 mmol) was added quickly dropwise. The reaction mixture was allowed to warm to 0° C. and was stirred for 30 min. The reaction mixture was cooled down to −78° C. 1,2-Dibromoethane (9.86 mL, 114 mmol) was added dropwise and the solution was allowed to warm to RT. The reaction mixture was quenched with 10 mL sat. aq. NH₄Cl. The mixture was partitioned between TBME (250 mL) and sat. aq. NH₄Cl (250 mL). The organic phase dried over Na₂SO₄, filtered and concentrated in vacuo to give 2-bromo-3-methoxy-6-neopentylnaphthalene as an orange solid (27.82 g, 70%).

DIPEA (82 ml, 470 mmol) and xantphos (7.77 g, 13.43 mmol) were added to a solution of 2-bromo-3-methoxy-6-neopentylnaphthalene (55 g, 134 mmol) in 1,4-dioxane (407 mL). The reaction mixture was degassed with bubbling nitrogen for 25 minutes. After this time, ethyl 3-mercaptopropanoate (20.42 ml, 161 mmol) and Pd₂(dba)₃ (6.15 g, 6.71 mmol) was added and the mixture was placed under nitrogen with a vacuum/nitrogen purge (×3). The reaction mixture was then stirred at 90° C. for 24 hours. The mixture was allowed to cool to RT then concentrated in vacuo to give an oily residue. The crude was dry-loaded onto silica (100 g). The crude product was purified by column chromatography (Isolera, 350 g Sfar Biotage column, 0-10% EtOAc in Heptane over 12 CV) yielding ethyl 3-((3-methoxy-6-neopentylnaphthalen-2-yl)thio)propanoate as a yellow oil that slowly solidified (38 g, 65%).

A solution of ethyl 3-((3-methoxy-6-neopentylnaphthalen-2-yl)thio)propanoate (31.5 g, 87 mmol) in DCM (300 mL) was cooled to −78° C. (dry ice/acetone). Boron tribromide 1M in DCM (218 mL, 218 mmol) was added dropwise slowly then the reaction mixture was stirred for 1 hour. The mixture was quenched by addition of EtOH (50 mL) then water (50 mL). The mixture was separated between DCM (500 mL) and water (500 mL). The organics were washed with brine (500 mL), dried over Na₂SO₄, filtered and concentrated in vacuo to give ethyl 3-((3-hydroxy-6-neopentylnaphthalen-2-yl)thio)propanoate as an orange solid (29.5 g, quantitative yield).

A solution of ethyl 3-((3-hydroxy-6-neopentylnaphthalen-2-yl)thio)propanoate (29.5 g, 85 mmol) and triethylamine (35.6 mL, 255 mmol) in DCM (284 mL) was cooled to 0° C. (ice/water) and trifluoromethanesulfonic anhydride (21.45 ml, 128 mmol) was added dropwise over 10 min. The reaction mixture was stirred at 0° C. for 30 min. The mixture was quenched with water and then separated between DCM (100 mL) and water (100 mL). The combined organic phased was dried over Na₂SO₄, filtered and concentrated in vacuo to give a dark orange oily residue. The residue was purified by column chromatography (Isolera, wet loaded in DCM, 2×330 g, EtOAc in heptane 0-12% over 18 CV) yielded ethyl 3-((6-neopentyl-3-(((trifluoromethyl)sulfonyl)oxy)naphthalen-2-yl)thio)propanoate as a pale-yellow oil (29.52 g, 72%).

A solution of ethyl 3-((6-neopentyl-3-(((trifluoromethyl)sulfonyl)oxy)naphthalen-2-yl)thio)propanoate (18.3 g, 38.2 mmol), and triethylamine anhydrous (25.4 mL, 191 mmol) in DCE (191 mL) was degassed with nitrogen for 30 min. The flask was placed under nitrogen then Pd(dppf)Cl₂-DCM (1.090 g, 1.338 mmol) was added. A suba-seal was added and 4,4,5,5-tetramethyl-1,3,2-dioxaborolane (16.65 mL, 115 mmol) added via syringe. The suba-seal was replaced with stopper, and the mixture heated at 88° C. (internal) for 30 minutes. The mixture was cooled in a water/ice bath then the excess HBpin quenched with IPA (10 mL). The mixture was concentrated in vacuo to give ethyl 3-((6-neopentyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thio)propanoate which was used crude in the next step.

A mixture of 2-chloro-3-fluoro-4-iodopyridine (10.83 g, 42.1 mmol), ethyl 3-((6-neopentyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)naphthalen-2-yl)thio)propanoate (17.46 g, 38.3 mmol) and potassium carbonate (13.22 g, 96 mmol) in 1,4-dioxane (106 mL) and water (21.25 mL) was sparged with nitrogen for 20 min. The reaction mixture was then heated to 110° C. under nitrogen for 12 hours. The mixture was allowed to cool to RT, then concentrated in vacuo. The crude was dissolved in DCM and dry-loaded onto silica (50 g) to purify by column chromatography to yield ethyl 3-((3-(2-chloro-3-fluoropyridin-4-yl)-6-neopentylnaphthalen-2-yl)thio)propanoate as a pale yellow oil (7.0 g, 40%).

A suspension of methyl 3-((3-(2-chloro-3-fluoropyridin-4-yl)-6-neopentylnaphthalen-2-yl)thio)propanoate (7 g, 15.70 mmol) and potassium tert-butoxide (2.64 g, 23.54 mmol) in anhydrous THF (105 ml) was stirred at RT for 15 minutes. The mixture was poured into EtOAc (400 mL) and 2M HCl (400 mL) then the layers were separated. The organics were washed with brine (200 mL), dried over MgSO₄, filtered and concentrated in vacuo to give 1-chloro-7-neopentylnaphtho[2′,3′:4,5]thieno[2,3-c]pyridine as a yellow solid (5.69 g, 90%).

A mixture of 1-chloro-7-neopentylnaphtho[2′,3′:4,5]thieno[2,3-c]pyridine (5.3 g, 15.59 mmol), (3,5-dimethylphenyl)boronic acid (4.68 g, 31.2 mmol) and potassium carbonate (4.31 g, 31.2 mmol) in 1,4-dioxane (65.0 mL) and water (12.99 mL) was sparged with nitrogen for 10 min. Tetrakis(triphenylphosphine)palladium(0) (0.901 g, 0.780 mmol) was added and the reaction mixture was heated at 110° C. for 2 hours. The reaction mixture was allowed to cool to RT then concentrated in vacuo. The crude was dissolved in DCM and dry loaded onto silica (50 g). The product was purified by column chromatography to yield a yellow solid (3.46 g, 30%).

To a solution were added iridium(III) chloride hydrate (1.112 g, 3.00 mmol, 1.0 equiv) and 1-(3,5-dimethyl-phenyl)-7-neopentylnaphtho[2′,3′:4,5]thieno[2,3-c]pyridine (1.966 g, 4.80 mmol, 1.6 equiv). The reaction mixture was sparged with nitrogen for 10 minutes then heated at 90° C. for 66 hours. The reaction mixture was cooled to RT, 3,7-diethylnonane-4,6-dione (1.274 g, 6.00 mmol, 4.0 equiv) and anhydrous tetrahydrofuran (30 mL) were added and the mixture sparged with nitrogen for 10 minutes. Powdered potassium carbonate (1.244 g, 9.00 mmol, 6.0 equiv) was added then the reaction mixture heated at 45° C. for 21 hours. The mixture was purified on silica gel to give product (1.16 g, 39% yield) as a red solid.

TABLE 1 Summary of photophysical properties of the inventive and comparative examples measured in PMMA. Excited state λmax FWHM lifetime PLQY (nm) (nm) (μs) (%) Inventive example 1 590 57 0.65 96 Inventive example 2 636 60 0.74 92 Inventive example 3 608 58 0.67 92 Inventive example 4 625 70 0.72 87 Inventive example 5 606 56 0.82 93 Comparative example 1 591 88 2.65 80

As shown in Table 1. Inventive examples 1 to 5 exhibited saturated red color with red shifted emission peak wavelength and narrower emission spectra (smaller FWHM). In addition, the Inventive examples have higher PLQYs and shorter excited state lifetime, which are superior properties for using them as emissive dopants in organic electroluminescence devices.

DEVICE EXAMPLES

All example devices were fabricated by high vacuum (<10⁻⁷ Torr) thermal evaporation. The anode electrode was 1,200 Å of indium tin oxide (ITO). The cathode consisted of 10 Å of Liq (8-hydroxyquinoline lithium) followed by 1,000 Å of Al. All devices were encapsulated with a glass lid sealed with an epoxy resin in a nitrogen glove box (<1 ppm of H₂O and O₂) immediately after fabrication, and a moisture getter was incorporated inside the package. The organic stack of the device examples consisted of sequentially, from the ITO surface, 100 Å of LG101 (purchased from LG Chem) as the hole injection layer (HIL); 400 Å of HTM as a hole transporting layer (HTL); 50 Å of EBM as an electron blocking layer (EBL); 400 Å of an emissive layer (EML) containing RH1 and 18% RH2 as red host and 3% of emitter, and 350 Å of Liq (8-hydroxyquinolinelithium) doped with 35% of ETM as the electron transporting layer (ETL). Table 1 shows the thickness of the device layers and materials.

TABLE 1 Device layer materials and thicknesses Layer Material Thickness [Å] Anode ITO 1,200 HIL LG101 100 HTL HTM 400 EBL EBM 50 EML RH1:RH2 18%:Red emitter 3% 400 ETL Liq:ETM 35% 350 EIL Liq 10 Cathode Al 1,000 The chemical structures of the device materials are shown below:

Upon fabrication, the devices were tested for electroluminescense (EL) and current-voltage-luminescence (JVL) characteristics. For this purpose, each sample device was energized by the 2 channel Keysight B2902A SMU at a current density of 10 mA/cm² and measured by the Photo Research PR735 Spectroradiometer. Radiance (W/str/cm²) from 380 nm to 1080 nm, and total integrated photon count were collected. The devices were then placed under a large area silicon photodiode for the JVL sweep. The integrated photon count of the device at 10 mA/cm² is used to convert the photodiode current to photon count. The voltage is swept from 0 to a voltage equating to 200 mA/cm². The EQE of the device is calculated using the total integrated photon count. LT95 is time of the luminescence decaying to 95% of the initial value measured at 80 mA/cm². All results are summarized in Table 2.

TABLE 2 λ max FWHM At 10 mA/cm² LT95 Device Red emitter [nm] [nm] Voltage [V] EQE [%] LE[cd/A] [h] Device 1 Inventive 642 57 4.0 29.3 18.0 195 example 2 Device 2 Inventive 629 56 3.9 29.3 27.1 248 example 4

Table 2 is a summary of performance of electroluminescence devices. The inventive devices showed saturated red color with high EQE and good device LT. 

What is claimed is:
 1. A compound comprising a first ligand L_(A) of Formula I,

wherein ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring; wherein K is selected from the group consisting of a direct bond, O, S, NR′, CR′R″, and SiR′R″; wherein two adjacent ones of X¹ to X⁴ are C and are fused to form a structure of Formula II,

wherein the dashed lines indicate direct bonds to ring B; wherein each of X¹ to X¹² independently represents C, CR or N, and each R can be same or different; wherein X is selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, Ge′RR″, SnR′R″, BR′, PR′, SbR′, and BiR′; wherein R^(A) represent mono to the maximum allowable substitution, or no substitution; wherein each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, selenyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein L_(A) is coordinated to a metal M through the indicated dashed lines; wherein the metal M has an atomic mass greater than 40; wherein the metal M can be coordinated to other ligands; wherein L_(A) may be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and wherein any two adjacent R, R′, R″, and R^(A) can be joined or fused to form a ring, with the proviso that that (1) when X is CR′R″, X⁵ is CR; and (2) when X is O, S, Se, or NR′, at least one of the following is true: (a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand; (b) at least one R comprises an electron withdrawing group; (c) at least two R^(A) is not hydrogen or deuterium; or (d) at least one R is selected from the group consisting of the structures of LIST 1 as defined herein.
 2. The compound of claim 1, wherein each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof.
 3. The compound of claim 1, wherein K is a direct bond or O.
 4. The compound of claim 1, wherein X¹ and X² are CR and the R_(s) are fused to form a structure of Formula II; or X² and X³ are CR and the R_(s) are fused to form a structure of Formula II; or X³ and X⁴ are CR and the R_(s) are fused to form a structure of Formula II.
 5. The compound of claim 1, wherein L_(A) has the structure

and each of R^(A1), R^(A2), R^(A3), and R^(A4) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof.
 6. The compound of claim 1, wherein X is CR′R″, and X⁵ is CR.
 7. The compound of claim 1, wherein the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand; or at least one R comprises an electron withdrawing group; or at least one R is selected from the group consisting of the structures of LIST 1 as defined herein.
 8. The compound of claim 1, wherein at least one of X¹ to X¹² is N; or each of X¹ to X¹² is CR.
 9. The compound of claim 1, wherein X is selected from the group consisting of O, S, Se, and NR′, wherein (a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand; or (b) at least one R comprises an electron withdrawing group; or (c) at least two R^(A) is not hydrogen or deuterium; or (d) at least one R is selected from the group consisting of:


10. The compound of claim 1, wherein the ligand L_(A) is has a structure of L_(Ai-m-X), where i is an integer from 1 to 4524, m is an integer from 1 to 184, and X is an integer from 1 to 4, wherein each of L_(Ai-1-X) to L_(Ai-184-X) has the structure defined below:

wherein when X in L_(Ai-m-X) is 1 it represents X in the above shown structures being O, when X in L_(Ai-m-X) is 2 it represents X in the above shown structures being S, when X in L_(Ai-m-X) is 3 it represents X in the above shown structures being Se, and when X in L_(Ai-m-X) is 4 it represents X in the above shown structures being NCH₃; wherein for each i in L_(Ai-m-X), R^(E) and G are defined as shown below: i R^(E) G i R^(E) G i R^(E) G i R^(E) G 1 R¹ G¹ 2 R¹ G² 3 R¹ G³ 4 R¹ G⁴ 5 R² G¹ 6 R² G² 7 R² G³ 8 R² G⁴ 9 R³ G¹ 10 R³ G² 11 R³ G³ 12 R³ G⁴ 13 R⁴ G¹ 14 R⁴ G² 15 R⁴ G³ 16 R⁴ G⁴ 17 R⁵ G¹ 18 R⁵ G² 19 R⁵ G³ 20 R⁵ G⁴ 21 R⁶ G¹ 22 R⁶ G² 23 R⁶ G³ 24 R⁶ G⁴ 25 R⁷ G¹ 26 R⁷ G² 27 R⁷ G³ 28 R⁷ G⁴ 29 R⁸ G¹ 30 R⁸ G² 31 R⁸ G³ 32 R⁸ G⁴ 33 R⁹ G¹ 34 R⁹ G² 35 R⁹ G³ 36 R⁹ G⁴ 37 R¹⁰ G¹ 38 R¹⁰ G² 39 R¹⁰ G³ 40 R¹⁰ G⁴ 41 R¹¹ G¹ 42 R¹¹ G² 43 R¹¹ G³ 44 R¹¹ G⁴ 45 R¹² G¹ 46 R¹² G² 47 R¹² G³ 48 R¹² G⁴ 49 R¹³ G¹ 50 R¹³ G² 51 R¹³ G³ 52 R¹³ G⁴ 53 R¹⁴ G¹ 54 R¹⁴ G² 55 R¹⁴ G³ 56 R¹⁴ G⁴ 57 R¹⁵ G¹ 58 R¹⁵ G² 59 R¹⁵ G³ 60 R¹⁵ G⁴ 61 R¹⁶ G¹ 62 R¹⁶ G² 63 R¹⁶ G³ 64 R¹⁶ G⁴ 65 R¹⁷ G¹ 66 R¹⁷ G² 67 R¹⁷ G³ 68 R¹⁷ G⁴ 69 R¹⁸ G¹ 70 R¹⁸ G² 71 R¹⁸ G³ 72 R¹⁸ G⁴ 73 R¹⁹ G¹ 74 R¹⁹ G² 75 R¹⁹ G³ 76 R¹⁹ G⁴ 77 R²⁰ G¹ 78 R²⁰ G² 79 R²⁰ G³ 80 R²⁰ G⁴ 81 R²¹ G¹ 82 R²¹ G² 83 R²¹ G³ 84 R²¹ G⁴ 85 R²² G¹ 86 R²² G² 87 R²² G³ 88 R²² G⁴ 89 R²³ G¹ 90 R²³ G² 91 R²³ G³ 92 R²³ G⁴ 93 R²⁴ G¹ 94 R²⁴ G² 95 R²⁴ G³ 96 R²⁴ G⁴ 97 R²⁵ G¹ 98 R²⁵ G² 99 R²⁵ G³ 100 R²⁵ G⁴ 101 R²⁶ G¹ 102 R²⁶ G² 103 R²⁶ G³ 104 R²⁶ G⁴ 105 R²⁷ G¹ 106 R²⁷ G² 107 R²⁷ G³ 108 R²⁷ G⁴ 109 R²⁸ G¹ 110 R²⁸ G² 111 R²⁸ G³ 112 R²⁸ G⁴ 113 R²⁹ G¹ 114 R²⁹ G² 115 R²⁹ G³ 116 R²⁹ G⁴ 117 R³⁰ G¹ 118 R³⁰ G² 119 R³⁰ G³ 120 R³⁰ G⁴ 121 R³¹ G¹ 122 R³¹ G² 123 R³¹ G³ 124 R³¹ G⁴ 125 R³² G¹ 126 R³² G² 127 R³² G³ 128 R³² G⁴ 129 R³³ G¹ 130 R³³ G² 131 R³³ G³ 132 R³³ G⁴ 133 R³⁴ G¹ 134 R³⁴ G² 135 R³⁴ G³ 136 R³⁴ G⁴ 137 R³⁵ G¹ 138 R³⁵ G² 139 R³⁵ G³ 140 R³⁵ G⁴ 141 R³⁶ G¹ 142 R³⁶ G² 143 R³⁶ G³ 144 R³⁶ G⁴ 145 R³⁷ G¹ 146 R³⁷ G² 147 R³⁷ G³ 148 R³⁷ G⁴ 149 R³⁸ G¹ 150 R³⁸ G² 151 R³⁸ G³ 152 R³⁸ G⁴ 153 R³⁹ G¹ 154 R³⁹ G² 155 R³⁹ G³ 156 R³⁹ G⁴ 157 R⁴⁰ G¹ 158 R⁴⁰ G² 159 R⁴⁰ G³ 160 R⁴⁰ G⁴ 161 R⁴¹ G¹ 162 R⁴¹ G² 163 R⁴¹ G³ 164 R⁴¹ G⁴ 165 R⁴² G¹ 166 R⁴² G² 167 R⁴² G³ 168 R⁴² G⁴ 169 R⁴³ G¹ 170 R⁴³ G² 171 R⁴³ G³ 172 R⁴³ G⁴ 173 R⁴⁴ G¹ 174 R⁴⁴ G² 175 R⁴⁴ G³ 176 R⁴⁴ G⁴ 177 R⁴⁵ G¹ 178 R⁴⁵ G² 179 R⁴⁵ G³ 180 R⁴⁵ G⁴ 181 R⁴⁶ G¹ 182 R⁴⁶ G² 183 R⁴⁶ G³ 184 R⁴⁶ G⁴ 185 R⁴⁷ G¹ 186 R⁴⁷ G² 187 R⁴⁷ G³ 188 R⁴⁷ G⁴ 189 R⁴⁸ G¹ 190 R⁴⁸ G² 191 R⁴⁸ G³ 192 R⁴⁸ G⁴ 193 R⁴⁹ G¹ 194 R⁴⁹ G² 195 R⁴⁹ G³ 196 R⁴⁹ G⁴ 197 R⁵⁰ G¹ 198 R⁵⁰ G² 199 R⁵⁰ G³ 200 R⁵⁰ G⁴ 201 R⁵¹ G¹ 202 R⁵¹ G² 203 R⁵¹ G³ 204 R⁵¹ G⁴ 205 R⁵² G¹ 206 R⁵² G² 207 R⁵² G³ 208 R⁵² G⁴ 209 R⁵³ G¹ 210 R⁵³ G² 211 R⁵³ G³ 212 R⁵³ G⁴ 213 R⁵⁴ G¹ 214 R⁵⁴ G² 215 R⁵⁴ G³ 216 R⁵⁴ G⁴ 217 R⁵⁵ G¹ 218 R⁵⁵ G² 219 R⁵⁵ G³ 220 R⁵⁵ G⁴ 221 R⁵⁶ G¹ 222 R⁵⁶ G² 223 R⁵⁶ G³ 224 R⁵⁶ G⁴ 225 R⁵⁷ G¹ 226 R⁵⁷ G² 227 R⁵⁷ G³ 228 R⁵⁷ G⁴ 229 R⁵⁸ G¹ 230 R⁵⁸ G² 231 R⁵⁸ G³ 232 R⁵⁸ G⁴ 233 R⁵⁹ G¹ 234 R⁵⁹ G² 235 R⁵⁹ G³ 236 R⁵⁹ G⁴ 237 R⁶⁰ G¹ 238 R⁶⁰ G² 239 R⁶⁰ G³ 240 R⁶⁰ G⁴ 241 R⁶¹ G¹ 242 R⁶¹ G² 243 R⁶¹ G³ 244 R⁶¹ G⁴ 245 R⁶² G¹ 246 R⁶² G² 247 R⁶² G³ 248 R⁶² G⁴ 249 R⁶³ G¹ 250 R⁶³ G² 251 R⁶³ G³ 252 R⁶³ G⁴ 253 R⁶⁴ G¹ 254 R⁶⁴ G² 255 R⁶⁴ G³ 256 R⁶⁴ G⁴ 257 R⁶⁵ G¹ 258 R⁶⁵ G² 259 R⁶⁵ G³ 260 R⁶⁵ G⁴ 261 R⁶⁶ G¹ 262 R⁶⁶ G² 263 R⁶⁶ G³ 264 R⁶⁶ G⁴ 265 R⁶⁷ G¹ 266 R⁶⁷ G² 267 R⁶⁷ G³ 268 R⁶⁷ G⁴ 269 R⁶⁸ G¹ 270 R⁶⁸ G² 271 R⁶⁸ G³ 272 R⁶⁸ G⁴ 273 R⁶⁹ G¹ 274 R⁶⁹ G² 275 R⁶⁹ G³ 276 R⁶⁹ G⁴ 277 R⁷⁰ G¹ 278 R⁷⁰ G² 279 R⁷⁰ G³ 280 R⁷⁰ G⁴ 281 R⁷¹ G¹ 282 R⁷¹ G² 283 R⁷¹ G³ 284 R⁷¹ G⁴ 285 R⁷² G¹ 286 R⁷² G² 287 R⁷² G³ 288 R⁷² G⁴ 289 R⁷³ G¹ 290 R⁷³ G² 291 R⁷³ G³ 292 R⁷³ G⁴ 293 R⁷⁴ G¹ 294 R⁷⁴ G² 295 R⁷⁴ G³ 296 R⁷⁴ G⁴ 297 R⁷⁵ G¹ 298 R⁷⁵ G² 299 R⁷⁵ G³ 300 R⁷⁵ G⁴ 301 R⁷⁶ G¹ 302 R⁷⁶ G² 303 R⁷⁶ G³ 304 R⁷⁶ G⁴ 305 R⁷⁷ G¹ 306 R⁷⁷ G² 307 R⁷⁷ G³ 308 R⁷⁷ G⁴ 309 R⁷⁸ G¹ 310 R⁷⁸ G² 311 R⁷⁸ G³ 312 R⁷⁸ G⁴ 313 R⁷⁹ G¹ 314 R⁷⁹ G² 315 R⁷⁹ G³ 316 R⁷⁹ G⁴ 317 R⁸⁰ G¹ 318 R⁸⁰ G² 319 R⁸⁰ G³ 320 R⁸⁰ G⁴ 321 R⁸¹ G¹ 322 R⁸¹ G² 323 R⁸¹ G³ 324 R⁸¹ G⁴ 325 R⁸² G¹ 326 R⁸² G² 327 R⁸² G³ 328 R⁸² G⁴ 329 R⁸³ G¹ 330 R⁸³ G² 331 R⁸³ G³ 332 R⁸³ G⁴ 333 R⁸⁴ G¹ 334 R⁸⁴ G² 335 R⁸⁴ G³ 336 R⁸⁴ G⁴ 337 R⁸⁵ G¹ 338 R⁸⁵ G² 339 R⁸⁵ G³ 340 R⁸⁵ G⁴ 341 R⁸⁶ G¹ 342 R⁸⁶ G² 343 R⁸⁶ G³ 344 R⁸⁶ G⁴ 345 R⁸⁷ G¹ 346 R⁸⁷ G² 347 R⁸⁷ G³ 348 R⁸⁷ G⁴ 349 R¹ G⁵ 350 R¹ G⁶ 351 R¹ G⁷ 352 R¹ G⁸ 353 R² G⁵ 354 R² G⁶ 355 R² G⁷ 356 R² G⁸ 357 R³ G⁵ 358 R³ G⁶ 359 R³ G⁷ 360 R³ G⁸ 361 R⁴ G⁵ 362 R⁴ G⁶ 363 R⁴ G⁷ 364 R⁴ G⁸ 365 R⁵ G⁵ 366 R⁵ G⁶ 367 R⁵ G⁷ 368 R⁵ G⁸ 369 R⁶ G⁵ 370 R⁶ G⁶ 371 R⁶ G⁷ 372 R⁶ G⁸ 373 R⁷ G⁵ 374 R⁷ G⁶ 375 R⁷ G⁷ 376 R⁷ G⁸ 377 R⁸ G⁵ 378 R⁸ G⁶ 379 R⁸ G⁷ 380 R⁸ G⁸ 381 R⁹ G⁵ 382 R⁹ G⁶ 383 R⁹ G⁷ 384 R⁹ G⁸ 385 R¹⁰ G⁵ 386 R¹⁰ G⁶ 387 R¹⁰ G⁷ 388 R¹⁰ G⁸ 389 R¹¹ G⁵ 390 R¹¹ G⁶ 391 R¹¹ G⁷ 392 R¹¹ G⁸ 393 R¹² G⁵ 394 R¹² G⁶ 395 R¹² G⁷ 396 R¹² G⁸ 397 R¹³ G⁵ 398 R¹³ G⁶ 399 R¹³ G⁷ 400 R¹³ G⁸ 401 R¹⁴ G⁵ 402 R¹⁴ G⁶ 403 R¹⁴ G⁷ 404 R¹⁴ G⁸ 405 R¹⁵ G⁵ 406 R¹⁵ G⁶ 407 R¹⁵ G⁷ 408 R¹⁵ G⁸ 409 R¹⁶ G⁵ 410 R¹⁶ G⁶ 411 R¹⁶ G⁷ 412 R¹⁶ G⁸ 413 R¹⁷ G⁵ 414 R¹⁷ G⁶ 415 R¹⁷ G⁷ 416 R¹⁷ G⁸ 417 R¹⁸ G⁵ 418 R¹⁸ G⁶ 419 R¹⁸ G⁷ 420 R¹⁸ G⁸ 421 R¹⁹ G⁵ 422 R¹⁹ G⁶ 423 R¹⁹ G⁷ 424 R¹⁹ G⁸ 425 R²⁰ G⁵ 426 R²⁰ G⁶ 427 R²⁰ G⁷ 428 R²⁰ G⁸ 429 R²¹ G⁵ 430 R²¹ G⁶ 431 R²¹ G⁷ 432 R²¹ G⁸ 433 R²² G⁵ 434 R²² G⁶ 435 R²² G⁷ 436 R²² G⁸ 437 R²³ G⁵ 438 R²³ G⁶ 439 R²³ G⁷ 440 R²³ G⁸ 441 R²⁴ G⁵ 442 R²⁴ G⁶ 443 R²⁴ G⁷ 444 R²⁴ G⁸ 445 R²⁵ G⁵ 446 R²⁵ G⁶ 447 R²⁵ G⁷ 448 R²⁵ G⁸ 449 R²⁶ G⁵ 450 R²⁶ G⁶ 451 R²⁶ G⁷ 452 R²⁶ G⁸ 453 R²⁷ G⁵ 454 R²⁷ G⁶ 455 R²⁷ G⁷ 456 R²⁷ G⁸ 457 R²⁸ G⁵ 458 R²⁸ G⁶ 459 R²⁸ G⁷ 460 R²⁸ G⁸ 461 R²⁹ G⁵ 462 R²⁹ G⁶ 463 R²⁹ G⁷ 464 R²⁹ G⁸ 465 R³⁰ G⁵ 466 R³⁰ G⁶ 467 R³⁰ G⁷ 468 R³⁰ G⁸ 469 R³¹ G⁵ 470 R³¹ G⁶ 471 R³¹ G⁷ 472 R³¹ G⁸ 473 R³² G⁵ 474 R³² G⁶ 475 R³² G⁷ 476 R³² G⁸ 477 R³³ G⁵ 478 R³³ G⁶ 479 R³³ G⁷ 480 R³³ G⁸ 481 R³⁴ G⁵ 482 R³⁴ G⁶ 483 R³⁴ G⁷ 484 R³⁴ G⁸ 485 R³⁵ G⁵ 486 R³⁵ G⁶ 487 R³⁵ G⁷ 488 R³⁵ G⁸ 489 R³⁶ G⁵ 490 R³⁶ G⁶ 491 R³⁶ G⁷ 492 R³⁶ G⁸ 493 R³⁷ G⁵ 494 R³⁷ G⁶ 495 R³⁷ G⁷ 496 R³⁷ G⁸ 497 R³⁸ G⁵ 498 R³⁸ G⁶ 499 R³⁸ G⁷ 500 R³⁸ G⁸ 501 R³⁹ G⁵ 502 R³⁹ G⁶ 503 R³⁹ G⁷ 504 R³⁹ G⁸ 505 R⁴⁰ G⁵ 506 R⁴⁰ G⁶ 507 R⁴⁰ G⁷ 508 R⁴⁰ G⁸ 509 R⁴¹ G⁵ 510 R⁴¹ G⁶ 511 R⁴¹ G⁷ 512 R⁴¹ G⁸ 513 R⁴² G⁵ 514 R⁴² G⁶ 515 R⁴² G⁷ 516 R⁴² G⁸ 517 R⁴³ G⁵ 518 R⁴³ G⁶ 519 R⁴³ G⁷ 520 R⁴³ G⁸ 521 R⁴⁴ G⁵ 522 R⁴⁴ G⁶ 523 R⁴⁴ G⁷ 524 R⁴⁴ G⁸ 525 R⁴⁵ G⁵ 526 R⁴⁵ G⁶ 527 R⁴⁵ G⁷ 528 R⁴⁵ G⁸ 529 R⁴⁶ G⁵ 530 R⁴⁶ G⁶ 531 R⁴⁶ G⁷ 532 R⁴⁶ G⁸ 533 R⁴⁷ G⁵ 534 R⁴⁷ G⁶ 535 R⁴⁷ G⁷ 536 R⁴⁷ G⁸ 537 R⁴⁸ G⁵ 538 R⁴⁸ G⁶ 539 R⁴⁸ G⁷ 540 R⁴⁸ G⁸ 541 R⁴⁹ G⁵ 542 R⁴⁹ G⁶ 543 R⁴⁹ G⁷ 544 R⁴⁹ G⁸ 545 R⁵⁰ G⁵ 546 R⁵⁰ G⁶ 547 R⁵⁰ G⁷ 548 R⁵⁰ G⁸ 549 R⁵¹ G⁵ 550 R⁵¹ G⁶ 551 R⁵¹ G⁷ 552 R⁵¹ G⁸ 553 R⁵² G⁵ 554 R⁵² G⁶ 555 R⁵² G⁷ 556 R⁵² G⁸ 557 R⁵³ G⁵ 558 R⁵³ G⁶ 559 R⁵³ G⁷ 560 R⁵³ G⁸ 561 R⁵⁴ G⁵ 562 R⁵⁴ G⁶ 563 R⁵⁴ G⁷ 564 R⁵⁴ G⁸ 565 R⁵⁵ G⁵ 566 R⁵⁵ G⁶ 567 R⁵⁵ G⁷ 568 R⁵⁵ G⁸ 569 R⁵⁶ G⁵ 570 R⁵⁶ G⁶ 571 R⁵⁶ G⁷ 572 R⁵⁶ G⁸ 573 R⁵⁷ G⁵ 574 R⁵⁷ G⁶ 575 R⁵⁷ G⁷ 576 R⁵⁷ G⁸ 577 R⁵⁸ G⁵ 578 R⁵⁸ G⁶ 579 R⁵⁸ G⁷ 580 R⁵⁸ G⁸ 581 R⁵⁹ G⁵ 582 R⁵⁹ G⁶ 583 R⁵⁹ G⁷ 584 R⁵⁹ G⁸ 585 R⁶⁰ G⁵ 586 R⁶⁰ G⁶ 587 R⁶⁰ G⁷ 588 R⁶⁰ G⁸ 589 R⁶¹ G⁵ 590 R⁶¹ G⁶ 591 R⁶¹ G⁷ 592 R⁶¹ G⁸ 593 R⁶² G⁵ 594 R⁶² G⁶ 595 R⁶² G⁷ 596 R⁶² G⁸ 597 R⁶³ G⁵ 598 R⁶³ G⁶ 599 R⁶³ G⁷ 600 R⁶³ G⁸ 601 R⁶⁴ G⁵ 602 R⁶⁴ G⁶ 603 R⁶⁴ G⁷ 604 R⁶⁴ G⁸ 605 R⁶⁵ G⁵ 606 R⁶⁵ G⁶ 607 R⁶⁵ G⁷ 608 R⁶⁵ G⁸ 609 R⁶⁶ G⁵ 610 R⁶⁶ G⁶ 611 R⁶⁶ G⁷ 612 R⁶⁶ G⁸ 613 R⁶⁷ G⁵ 614 R⁶⁷ G⁶ 615 R⁶⁷ G⁷ 616 R⁶⁷ G⁸ 617 R⁶⁸ G⁵ 618 R⁶⁸ G⁶ 619 R⁶⁸ G⁷ 620 R⁶⁸ G⁸ 621 R⁶⁹ G⁵ 622 R⁶⁹ G⁶ 623 R⁶⁹ G⁷ 624 R⁶⁹ G⁸ 625 R⁷⁰ G⁵ 626 R⁷⁰ G⁶ 627 R⁷⁰ G⁷ 628 R⁷⁰ G⁸ 629 R⁷¹ G⁵ 630 R⁷¹ G⁶ 631 R⁷¹ G⁷ 632 R⁷¹ G⁸ 633 R⁷² G⁵ 634 R⁷² G⁶ 635 R⁷² G⁷ 636 R⁷² G⁸ 637 R⁷³ G⁵ 638 R⁷³ G⁶ 639 R⁷³ G⁷ 640 R⁷³ G⁸ 641 R⁷⁴ G⁵ 642 R⁷⁴ G⁶ 643 R⁷⁴ G⁷ 644 R⁷⁴ G⁸ 645 R⁷⁵ G⁵ 646 R⁷⁵ G⁶ 647 R⁷⁵ G⁷ 648 R⁷⁵ G⁸ 649 R⁷⁶ G⁵ 650 R⁷⁶ G⁶ 651 R⁷⁶ G⁷ 652 R⁷⁶ G⁸ 653 R⁷⁷ G⁵ 654 R⁷⁷ G⁶ 655 R⁷⁷ G⁷ 656 R⁷⁷ G⁸ 657 R⁷⁸ G⁵ 658 R⁷⁸ G⁶ 659 R⁷⁸ G⁷ 660 R⁷⁸ G⁸ 661 R⁷⁹ G⁵ 662 R⁷⁹ G⁶ 663 R⁷⁹ G⁷ 664 R⁷⁹ G⁸ 665 R⁸⁰ G⁵ 666 R⁸⁰ G⁶ 667 R⁸⁰ G⁷ 668 R⁸⁰ G⁸ 669 R⁸¹ G⁵ 670 R⁸¹ G⁶ 671 R⁸¹ G⁷ 672 R⁸¹ G⁸ 673 R⁸² G⁵ 674 R⁸² G⁶ 675 R⁸² G⁷ 676 R⁸² G⁸ 677 R⁸³ G⁵ 678 R⁸³ G⁶ 679 R⁸³ G⁷ 680 R⁸³ G⁸ 681 R⁸⁴ G⁵ 682 R⁸⁴ G⁶ 683 R⁸⁴ G⁷ 684 R⁸⁴ G⁸ 685 R⁸⁵ G⁵ 686 R⁸⁵ G⁶ 687 R⁸⁵ G⁷ 688 R⁸⁵ G⁸ 689 R⁸⁶ G⁵ 690 R⁸⁶ G⁶ 691 R⁸⁶ G⁷ 692 R⁸⁶ G⁸ 693 R⁸⁷ G⁵ 694 R⁸⁷ G⁶ 695 R⁸⁷ G⁷ 696 R⁸⁷ G⁸ 697 R¹ G⁹ 698 R¹ G¹⁰ 699 R¹ G¹¹ 700 R¹ G¹² 701 R² G⁹ 702 R² G¹⁰ 703 R² G¹¹ 704 R² G¹² 705 R³ G⁹ 706 R³ G¹⁰ 707 R³ G¹¹ 708 R³ G¹² 709 R⁴ G⁹ 710 R⁴ G¹⁰ 711 R⁴ G¹¹ 712 R⁴ G¹² 713 R⁵ G⁹ 714 R⁵ G¹⁰ 715 R⁵ G¹¹ 716 R⁵ G¹² 717 R⁶ G⁹ 718 R⁶ G¹⁰ 719 R⁶ G¹¹ 720 R⁶ G¹² 721 R⁷ G⁹ 722 R⁷ G¹⁰ 723 R⁷ G¹¹ 724 R⁷ G¹² 725 R⁸ G⁹ 726 R⁸ G¹⁰ 727 R⁸ G¹¹ 728 R⁸ G¹² 729 R⁹ G⁹ 730 R⁹ G¹⁰ 731 R⁹ G¹¹ 732 R⁹ G¹² 733 R¹⁰ G⁹ 734 R¹⁰ G¹⁰ 735 R¹⁰ G¹¹ 736 R¹⁰ G¹² 737 R¹¹ G⁹ 738 R¹¹ G¹⁰ 739 R¹¹ G¹¹ 740 R¹¹ G¹² 741 R¹² G⁹ 742 R¹² G¹⁰ 743 R¹² G¹¹ 744 R¹² G¹² 745 R¹³ G⁹ 746 R¹³ G¹⁰ 747 R¹³ G¹¹ 748 R¹³ G¹² 749 R¹⁴ G⁹ 750 R¹⁴ G¹⁰ 751 R¹⁴ G¹¹ 752 R¹⁴ G¹² 753 R¹⁵ G⁹ 754 R¹⁵ G¹⁰ 755 R¹⁵ G¹¹ 756 R¹⁵ G¹² 757 R¹⁶ G⁹ 758 R¹⁶ G¹⁰ 759 R¹⁶ G¹¹ 760 R¹⁶ G¹² 761 R¹⁷ G⁹ 762 R¹⁷ G¹⁰ 763 R¹⁷ G¹¹ 764 R¹⁷ G¹² 765 R¹⁸ G⁹ 766 R¹⁸ G¹⁰ 767 R¹⁸ G¹¹ 768 R¹⁸ G¹² 769 R¹⁹ G⁹ 770 R¹⁹ G¹⁰ 771 R¹⁹ G¹¹ 772 R¹⁹ G¹² 773 R²⁰ G⁹ 774 R²⁰ G¹⁰ 775 R²⁰ G¹¹ 776 R²⁰ G¹² 777 R²¹ G⁹ 778 R²¹ G¹⁰ 779 R²¹ G¹¹ 780 R²¹ G¹² 781 R²² G⁹ 782 R²² G¹⁰ 783 R²² G¹¹ 784 R²² G¹² 785 R²³ G⁹ 786 R²³ G¹⁰ 787 R²³ G¹¹ 788 R²³ G¹² 789 R²⁴ G⁹ 790 R²⁴ G¹⁰ 791 R²⁴ G¹¹ 792 R²⁴ G¹² 793 R²⁵ G⁹ 794 R²⁵ G¹⁰ 795 R²⁵ G¹¹ 796 R²⁵ G¹² 797 R²⁶ G⁹ 798 R²⁶ G¹⁰ 799 R²⁶ G¹¹ 800 R²⁶ G¹² 801 R²⁷ G⁹ 802 R²⁷ G¹⁰ 803 R²⁷ G¹¹ 804 R²⁷ G¹² 805 R²⁸ G⁹ 806 R²⁸ G¹⁰ 807 R²⁸ G¹¹ 808 R²⁸ G¹² 809 R²⁹ G⁹ 810 R²⁹ G¹⁰ 811 R²⁹ G¹¹ 812 R²⁹ G¹² 813 R³⁰ G⁹ 814 R³⁰ G¹⁰ 815 R³⁰ G¹¹ 816 R³⁰ G¹² 817 R³¹ G⁹ 818 R³¹ G¹⁰ 819 R³¹ G¹¹ 820 R³¹ G¹² 821 R³² G⁹ 822 R³² G¹⁰ 823 R³² G¹¹ 824 R³² G¹² 825 R³³ G⁹ 826 R³³ G¹⁰ 827 R³³ G¹¹ 828 R³³ G¹² 829 R³⁴ G⁹ 830 R³⁴ G¹⁰ 831 R³⁴ G¹¹ 832 R³⁴ G¹² 833 R³⁵ G⁹ 834 R³⁵ G¹⁰ 835 R³⁵ G¹¹ 836 R³⁵ G¹² 837 R³⁶ G⁹ 838 R³⁶ G¹⁰ 839 R³⁶ G¹¹ 840 R³⁶ G¹² 841 R³⁷ G⁹ 842 R³⁷ G¹⁰ 843 R³⁷ G¹¹ 844 R³⁷ G¹² 845 R³⁸ G⁹ 846 R³⁸ G¹⁰ 847 R³⁸ G¹¹ 848 R³⁸ G¹² 849 R³⁹ G⁹ 850 R³⁹ G¹⁰ 851 R³⁹ G¹¹ 852 R³⁹ G¹² 853 R⁴⁰ G⁹ 854 R⁴⁰ G¹⁰ 855 R⁴⁰ G¹¹ 856 R⁴⁰ G¹² 857 R⁴¹ G⁹ 858 R⁴¹ G¹⁰ 859 R⁴¹ G¹¹ 860 R⁴¹ G¹² 861 R⁴² G⁹ 862 R⁴² G¹⁰ 863 R⁴² G¹¹ 864 R⁴² G¹² 865 R⁴³ G⁹ 866 R⁴³ G¹⁰ 867 R⁴³ G¹¹ 868 R⁴³ G¹² 869 R⁴⁴ G⁹ 870 R⁴⁴ G¹⁰ 871 R⁴⁴ G¹¹ 872 R⁴⁴ G¹² 873 R⁴⁵ G⁹ 874 R⁴⁵ G¹⁰ 875 R⁴⁵ G¹¹ 876 R⁴⁵ G¹² 877 R⁴⁶ G⁹ 878 R⁴⁶ G¹⁰ 879 R⁴⁶ G¹¹ 880 R⁴⁶ G¹² 881 R⁴⁷ G⁹ 882 R⁴⁷ G¹⁰ 883 R⁴⁷ G¹¹ 884 R⁴⁷ G¹² 885 R⁴⁸ G⁹ 886 R⁴⁸ G¹⁰ 887 R⁴⁸ G¹¹ 888 R⁴⁸ G¹² 889 R⁴⁹ G⁹ 890 R⁴⁹ G¹⁰ 891 R⁴⁹ G¹¹ 892 R⁴⁹ G¹² 893 R⁵⁰ G⁹ 894 R⁵⁰ G¹⁰ 895 R⁵⁰ G¹¹ 896 R⁵⁰ G¹² 897 R⁵¹ G⁹ 898 R⁵¹ G¹⁰ 899 R⁵¹ G¹¹ 900 R⁵¹ G¹² 901 R⁵² G⁹ 902 R⁵² G¹⁰ 903 R⁵² G¹¹ 904 R⁵² G¹² 905 R⁵³ G⁹ 906 R⁵³ G¹⁰ 907 R⁵³ G¹¹ 908 R⁵³ G¹² 909 R⁵⁴ G⁹ 910 R⁵⁴ G¹⁰ 911 R⁵⁴ G¹¹ 912 R⁵⁴ G¹² 913 R⁵⁵ G⁹ 914 R⁵⁵ G¹⁰ 915 R⁵⁵ G¹¹ 916 R⁵⁵ G¹² 917 R⁵⁶ G⁹ 918 R⁵⁶ G¹⁰ 919 R⁵⁶ G¹¹ 920 R⁵⁶ G¹² 921 R⁵⁷ G⁹ 922 R⁵⁷ G¹⁰ 923 R⁵⁷ G¹¹ 924 R⁵⁷ G¹² 925 R⁵⁸ G⁹ 926 R⁵⁸ G¹⁰ 927 R⁵⁸ G¹¹ 928 R⁵⁸ G¹² 929 R⁵⁹ G⁹ 930 R⁵⁹ G¹⁰ 931 R⁵⁹ G¹¹ 932 R⁵⁹ G¹² 933 R⁶⁰ G⁹ 934 R⁶⁰ G¹⁰ 935 R⁶⁰ G¹¹ 936 R⁶⁰ G¹² 937 R⁶¹ G⁹ 938 R⁶¹ G¹⁰ 939 R⁶¹ G¹¹ 940 R⁶¹ G¹² 941 R⁶² G⁹ 942 R⁶² G¹⁰ 943 R⁶² G¹¹ 944 R⁶² G¹² 945 R⁶³ G⁹ 946 R⁶³ G¹⁰ 947 R⁶³ G¹¹ 948 R⁶³ G¹² 949 R⁶⁴ G⁹ 950 R⁶⁴ G¹⁰ 951 R⁶⁴ G¹¹ 952 R⁶⁴ G¹² 953 R⁶⁵ G⁹ 954 R⁶⁵ G¹⁰ 955 R⁶⁵ G¹¹ 956 R⁶⁵ G¹² 957 R⁶⁶ G⁹ 958 R⁶⁶ G¹⁰ 959 R⁶⁶ G¹¹ 960 R⁶⁶ G¹² 961 R⁶⁷ G⁹ 962 R⁶⁷ G¹⁰ 963 R⁶⁷ G¹¹ 964 R⁶⁷ G¹² 965 R⁶⁸ G⁹ 966 R⁶⁸ G¹⁰ 967 R⁶⁸ G¹¹ 968 R⁶⁸ G¹² 969 R⁶⁹ G⁹ 970 R⁶⁹ G¹⁰ 971 R⁶⁹ G¹¹ 972 R⁶⁹ G¹² 973 R⁷⁰ G⁹ 974 R⁷⁰ G¹⁰ 975 R⁷⁰ G¹¹ 976 R⁷⁰ G¹² 977 R⁷¹ G⁹ 978 R⁷¹ G¹⁰ 979 R⁷¹ G¹¹ 980 R⁷¹ G¹² 981 R⁷² G⁹ 982 R⁷² G¹⁰ 983 R⁷² G¹¹ 984 R⁷² G¹² 985 R⁷³ G⁹ 986 R⁷³ G¹⁰ 987 R⁷³ G¹¹ 988 R⁷³ G¹² 989 R⁷⁴ G⁹ 990 R⁷⁴ G¹⁰ 991 R⁷⁴ G¹¹ 992 R⁷⁴ G¹² 993 R⁷⁵ G⁹ 994 R⁷⁵ G¹⁰ 995 R⁷⁵ G¹¹ 996 R⁷⁵ G¹² 997 R⁷⁶ G⁹ 998 R⁷⁶ G¹⁰ 999 R⁷⁶ G¹¹ 1000 R⁷⁶ G¹² 1001 R⁷⁷ G⁹ 1002 R⁷⁷ G¹⁰ 1003 R⁷⁷ G¹¹ 1004 R⁷⁷ G¹² 1005 R⁷⁸ G⁹ 1006 R⁷⁸ G¹⁰ 1007 R⁷⁸ G¹¹ 1008 R⁷⁸ G¹² 1009 R⁷⁹ G⁹ 1010 R⁷⁹ G¹⁰ 1011 R⁷⁹ G¹¹ 1012 R⁷⁹ G¹² 1013 R⁸⁰ G⁹ 1014 R⁸⁰ G¹⁰ 1015 R⁸⁰ G¹¹ 1016 R⁸⁰ G¹² 1017 R⁸¹ G⁹ 1018 R⁸¹ G¹⁰ 1019 R⁸¹ G¹¹ 1020 R⁸¹ G¹² 1021 R⁸² G⁹ 1022 R⁸² G¹⁰ 1023 R⁸² G¹¹ 1024 R⁸² G¹² 1025 R⁸³ G⁹ 1026 R⁸³ G¹⁰ 1027 R⁸³ G¹¹ 1028 R⁸³ G¹² 1029 R⁸⁴ G⁹ 1030 R⁸⁴ G¹⁰ 1031 R⁸⁴ G¹¹ 1032 R⁸⁴ G¹² 1033 R⁸⁵ G⁹ 1034 R⁸⁵ G¹⁰ 1035 R⁸⁵ G¹¹ 1036 R⁸⁵ G¹² 1037 R⁸⁶ G⁹ 1038 R⁸⁶ G¹⁰ 1039 R⁸⁶ G¹¹ 1040 R⁸⁶ G¹² 1041 R⁸⁷ G⁹ 1042 R⁸⁷ G¹⁰ 1043 R⁸⁷ G¹¹ 1044 R⁸⁷ G¹² 1045 R¹ G¹³ 1046 R¹ G¹⁴ 1047 R¹ G¹⁵ 1048 R¹ G¹⁶ 1049 R² G¹³ 1050 R² G¹⁴ 1051 R² G¹⁵ 1052 R² G¹⁶ 1053 R³ G¹³ 1054 R³ G¹⁴ 1055 R³ G¹⁵ 1056 R³ G¹⁶ 1057 R⁴ G¹³ 1058 R⁴ G¹⁴ 1059 R⁴ G¹⁵ 1060 R⁴ G¹⁶ 1061 R⁵ G¹³ 1062 R⁵ G¹⁴ 1063 R⁵ G¹⁵ 1064 R⁵ G¹⁶ 1065 R⁶ G¹³ 1066 R⁶ G¹⁴ 1067 R⁶ G¹⁵ 1068 R⁶ G¹⁶ 1069 R⁷ G¹³ 1070 R⁷ G¹⁴ 1071 R⁷ G¹⁵ 1072 R⁷ G¹⁶ 1073 R⁸ G¹³ 1074 R⁸ G¹⁴ 1075 R⁸ G¹⁵ 1076 R⁸ G¹⁶ 1077 R⁹ G¹³ 1078 R⁹ G¹⁴ 1079 R⁹ G¹⁵ 1080 R⁹ G¹⁶ 1081 R¹⁰ G¹³ 1082 R¹⁰ G¹⁴ 1083 R¹⁰ G¹⁵ 1084 R¹⁰ G¹⁶ 1085 R¹¹ G¹³ 1086 R¹¹ G¹⁴ 1087 R¹¹ G¹⁵ 1088 R¹¹ G¹⁶ 1089 R¹² G¹³ 1090 R¹² G¹⁴ 1091 R¹² G¹⁵ 1092 R¹² G¹⁶ 1093 R¹³ G¹³ 1094 R¹³ G¹⁴ 1095 R¹³ G¹⁵ 1096 R¹³ G¹⁶ 1097 R¹⁴ G¹³ 1098 R¹⁴ G¹⁴ 1099 R¹⁴ G¹⁵ 1100 R¹⁴ G¹⁶ 1101 R¹⁵ G¹³ 1102 R¹⁵ G¹⁴ 1103 R¹⁵ G¹⁵ 1104 R¹⁵ G¹⁶ 1105 R¹⁶ G¹³ 1106 R¹⁶ G¹⁴ 1107 R¹⁶ G¹⁵ 1108 R¹⁶ G¹⁶ 1109 R¹⁷ G¹³ 1110 R¹⁷ G¹⁴ 1111 R¹⁷ G¹⁵ 1112 R¹⁷ G¹⁶ 1113 R¹⁸ G¹³ 1114 R¹⁸ G¹⁴ 1115 R¹⁸ G¹⁵ 1116 R¹⁸ G¹⁶ 1117 R¹⁹ G¹³ 1118 R¹⁹ G¹⁴ 1119 R¹⁹ G¹⁵ 1120 R¹⁹ G¹⁶ 1121 R²⁰ G¹³ 1122 R²⁰ G¹⁴ 1123 R²⁰ G¹⁵ 1124 R²⁰ G¹⁶ 1125 R²¹ G¹³ 1126 R²¹ G¹⁴ 1127 R²¹ G¹⁵ 1128 R²¹ G¹⁶ 1129 R²² G¹³ 1130 R²² G¹⁴ 1131 R²² G¹⁵ 1132 R²² G¹⁶ 1133 R²³ G¹³ 1134 R²³ G¹⁴ 1135 R²³ G¹⁵ 1136 R²³ G¹⁶ 1137 R²⁴ G¹³ 1138 R²⁴ G¹⁴ 1139 R²⁴ G¹⁵ 1140 R²⁴ G¹⁶ 1141 R²⁵ G¹³ 1142 R²⁵ G¹⁴ 1143 R²⁵ G¹⁵ 1144 R²⁵ G¹⁶ 1145 R²⁶ G¹³ 1146 R²⁶ G¹⁴ 1147 R²⁶ G¹⁵ 1148 R²⁶ G¹⁶ 1149 R²⁷ G¹³ 1150 R²⁷ G¹⁴ 1151 R²⁷ G¹⁵ 1152 R²⁷ G¹⁶ 1153 R²⁸ G¹³ 1154 R²⁸ G¹⁴ 1155 R²⁸ G¹⁵ 1156 R²⁸ G¹⁶ 1157 R²⁹ G¹³ 1158 R²⁹ G¹⁴ 1159 R²⁹ G¹⁵ 1160 R²⁹ G¹⁶ 1161 R³⁰ G¹³ 1162 R³⁰ G¹⁴ 1163 R³⁰ G¹⁵ 1164 R³⁰ G¹⁶ 1165 R³¹ G¹³ 1166 R³¹ G¹⁴ 1167 R³¹ G¹⁵ 1168 R³¹ G¹⁶ 1169 R³² G¹³ 1170 R³² G¹⁴ 1171 R³² G¹⁵ 1172 R³² G¹⁶ 1173 R³³ G¹³ 1174 R³³ G¹⁴ 1175 R³³ G¹⁵ 1176 R³³ G¹⁶ 1177 R³⁴ G¹³ 1178 R³⁴ G¹⁴ 1179 R³⁴ G¹⁵ 1180 R³⁴ G¹⁶ 1181 R³⁵ G¹³ 1182 R³⁵ G¹⁴ 1183 R³⁵ G¹⁵ 1184 R³⁵ G¹⁶ 1185 R³⁶ G¹³ 1186 R³⁶ G¹⁴ 1187 R³⁶ G¹⁵ 1188 R³⁶ G¹⁶ 1189 R³⁷ G¹³ 1190 R³⁷ G¹⁴ 1191 R³⁷ G¹⁵ 1192 R³⁷ G¹⁶ 1193 R³⁸ G¹³ 1194 R³⁸ G¹⁴ 1195 R³⁸ G¹⁵ 1196 R³⁸ G¹⁶ 1197 R³⁹ G¹³ 1198 R³⁹ G¹⁴ 1199 R³⁹ G¹⁵ 1200 R³⁹ G¹⁶ 1201 R⁴⁰ G¹³ 1202 R⁴⁰ G¹⁴ 1203 R⁴⁰ G¹⁵ 1204 R⁴⁰ G¹⁶ 1205 R⁴¹ G¹³ 1206 R⁴¹ G¹⁴ 1207 R⁴¹ G¹⁵ 1208 R⁴¹ G¹⁶ 1209 R⁴² G¹³ 1210 R⁴² G¹⁴ 1211 R⁴² G¹⁵ 1212 R⁴² G¹⁶ 1213 R⁴³ G¹³ 1214 R⁴³ G¹⁴ 1215 R⁴³ G¹⁵ 1216 R⁴³ G¹⁶ 1217 R⁴⁴ G¹³ 1218 R⁴⁴ G¹⁴ 1219 R⁴⁴ G¹⁵ 1220 R⁴⁴ G¹⁶ 1221 R⁴⁵ G¹³ 1222 R⁴⁵ G¹⁴ 1223 R⁴⁵ G¹⁵ 1224 R⁴⁵ G¹⁶ 1225 R⁴⁶ G¹³ 1226 R⁴⁶ G¹⁴ 1227 R⁴⁶ G¹⁵ 1228 R⁴⁶ G¹⁶ 1229 R⁴⁷ G¹³ 1230 R⁴⁷ G¹⁴ 1231 R⁴⁷ G¹⁵ 1232 R⁴⁷ G¹⁶ 1233 R⁴⁸ G¹³ 1234 R⁴⁸ G¹⁴ 1235 R⁴⁸ G¹⁵ 1236 R⁴⁸ G¹⁶ 1237 R⁴⁹ G¹³ 1238 R⁴⁹ G¹⁴ 1239 R⁴⁹ G¹⁵ 1240 R⁴⁹ G¹⁶ 1241 R⁵⁰ G¹³ 1242 R⁵⁰ G¹⁴ 1243 R⁵⁰ G¹⁵ 1244 R⁵⁰ G¹⁶ 1245 R⁵¹ G¹³ 1246 R⁵¹ G¹⁴ 1247 R⁵¹ G¹⁵ 1248 R⁵¹ G¹⁶ 1249 R⁵² G¹³ 1250 R⁵² G¹⁴ 1251 R⁵² G¹⁵ 1252 R⁵² G¹⁶ 1253 R⁵³ G¹³ 1254 R⁵³ G¹⁴ 1255 R⁵³ G¹⁵ 1256 R⁵³ G¹⁶ 1257 R⁵⁴ G¹³ 1258 R⁵⁴ G¹⁴ 1259 R⁵⁴ G¹⁵ 1260 R⁵⁴ G¹⁶ 1261 R⁵⁵ G¹³ 1262 R⁵⁵ G¹⁴ 1263 R⁵⁵ G¹⁵ 1264 R⁵⁵ G¹⁶ 1265 R⁵⁶ G¹³ 1266 R⁵⁶ G¹⁴ 1267 R⁵⁶ G¹⁵ 1268 R⁵⁶ G¹⁶ 1269 R⁵⁷ G¹³ 1270 R⁵⁷ G¹⁴ 1271 R⁵⁷ G¹⁵ 1272 R⁵⁷ G¹⁶ 1273 R⁵⁸ G¹³ 1274 R⁵⁸ G¹⁴ 1275 R⁵⁸ G¹⁵ 1276 R⁵⁸ G¹⁶ 1277 R⁵⁹ G¹³ 1278 R⁵⁹ G¹⁴ 1279 R⁵⁹ G¹⁵ 1280 R⁵⁹ G¹⁶ 1281 R⁶⁰ G¹³ 1282 R⁶⁰ G¹⁴ 1283 R⁶⁰ G¹⁵ 1284 R⁶⁰ G¹⁶ 1285 R⁶¹ G¹³ 1286 R⁶¹ G¹⁴ 1287 R⁶¹ G¹⁵ 1288 R⁶¹ G¹⁶ 1289 R⁶² G¹³ 1290 R⁶² G¹⁴ 1291 R⁶² G¹⁵ 1292 R⁶² G¹⁶ 1293 R⁶³ G¹³ 1294 R⁶³ G¹⁴ 1295 R⁶³ G¹⁵ 1296 R⁶³ G¹⁶ 1297 R⁶⁴ G¹³ 1298 R⁶⁴ G¹⁴ 1299 R⁶⁴ G¹⁵ 1300 R⁶⁴ G¹⁶ 1301 R⁶⁵ G¹³ 1302 R⁶⁵ G¹⁴ 1303 R⁶⁵ G¹⁵ 1304 R⁶⁵ G¹⁶ 1305 R⁶⁶ G¹³ 1306 R⁶⁶ G¹⁴ 1307 R⁶⁶ G¹⁵ 1308 R⁶⁶ G¹⁶ 1309 R⁶⁷ G¹³ 1310 R⁶⁷ G¹⁴ 1311 R⁶⁷ G¹⁵ 1312 R⁶⁷ G¹⁶ 1313 R⁶⁸ G¹³ 1314 R⁶⁸ G¹⁴ 1315 R⁶⁸ G¹⁵ 1316 R⁶⁸ G¹⁶ 1317 R⁶⁹ G¹³ 1318 R⁶⁹ G¹⁴ 1319 R⁶⁹ G¹⁵ 1320 R⁶⁹ G¹⁶ 1321 R⁷⁰ G¹³ 1322 R⁷⁰ G¹⁴ 1323 R⁷⁰ G¹⁵ 1324 R⁷⁰ G¹⁶ 1325 R⁷¹ G¹³ 1326 R⁷¹ G¹⁴ 1327 R⁷¹ G¹⁵ 1328 R⁷¹ G¹⁶ 1329 R⁷² G¹³ 1330 R⁷² G¹⁴ 1331 R⁷² G¹⁵ 1332 R⁷² G¹⁶ 1333 R⁷³ G¹³ 1334 R⁷³ G¹⁴ 1335 R⁷³ G¹⁵ 1336 R⁷³ G¹⁶ 1337 R⁷⁴ G¹³ 1338 R⁷⁴ G¹⁴ 1339 R⁷⁴ G¹⁵ 1340 R⁷⁴ G¹⁶ 1341 R⁷⁵ G¹³ 1342 R⁷⁵ G¹⁴ 1343 R⁷⁵ G¹⁵ 1344 R⁷⁵ G¹⁶ 1345 R⁷⁶ G¹³ 1346 R⁷⁶ G¹⁴ 1347 R⁷⁶ G¹⁵ 1348 R⁷⁶ G¹⁶ 1349 R⁷⁷ G¹³ 1350 R⁷⁷ G¹⁴ 1351 R⁷⁷ G¹⁵ 1352 R⁷⁷ G¹⁶ 1353 R⁷⁸ G¹³ 1354 R⁷⁸ G¹⁴ 1355 R⁷⁸ G¹⁵ 1356 R⁷⁸ G¹⁶ 1357 R⁷⁹ G¹³ 1358 R⁷⁹ G¹⁴ 1359 R⁷⁹ G¹⁵ 1360 R⁷⁹ G¹⁶ 1361 R⁸⁰ G¹³ 1362 R⁸⁰ G¹⁴ 1363 R⁸⁰ G¹⁵ 1364 R⁸⁰ G¹⁶ 1365 R⁸¹ G¹³ 1366 R⁸¹ G¹⁴ 1367 R⁸¹ G¹⁵ 1368 R⁸¹ G¹⁶ 1369 R⁸² G¹³ 1370 R⁸² G¹⁴ 1371 R⁸² G¹⁵ 1372 R⁸² G¹⁶ 1373 R⁸³ G¹³ 1374 R⁸³ G¹⁴ 1375 R⁸³ G¹⁵ 1376 R⁸³ G¹⁶ 1377 R⁸⁴ G¹³ 1378 R⁸⁴ G¹⁴ 1379 R⁸⁴ G¹⁵ 1380 R⁸⁴ G¹⁶ 1381 R⁸⁵ G¹³ 1382 R⁸⁵ G¹⁴ 1383 R⁸⁵ G¹⁵ 1384 R⁸⁵ G¹⁶ 1385 R⁸⁶ G¹³ 1386 R⁸⁶ G¹⁴ 1387 R⁸⁶ G¹⁵ 1388 R⁸⁶ G¹⁶ 1389 R⁸⁷ G¹³ 1390 R⁸⁷ G¹⁴ 1391 R⁸⁷ G¹⁵ 1392 R⁸⁷ G¹⁶ 1393 R¹ G¹⁷ 1394 R¹ G¹⁸ 1395 R¹ G¹⁹ 1396 R¹ G²⁰ 1397 R² G¹⁷ 1398 R² G¹⁸ 1399 R² G¹⁹ 1400 R² G²⁰ 1401 R³ G¹⁷ 1402 R³ G¹⁸ 1403 R³ G¹⁹ 1404 R³ G²⁰ 1405 R⁴ G¹⁷ 1406 R⁴ G¹⁸ 1407 R⁴ G¹⁹ 1408 R⁴ G²⁰ 1409 R⁵ G¹⁷ 1410 R⁵ G¹⁸ 1411 R⁵ G¹⁹ 1412 R⁵ G²⁰ 1413 R⁶ G¹⁷ 1414 R⁶ G¹⁸ 1415 R⁶ G¹⁹ 1416 R⁶ G²⁰ 1417 R⁷ G¹⁷ 1418 R⁷ G¹⁸ 1419 R⁷ G¹⁹ 1420 R⁷ G²⁰ 1421 R⁸ G¹⁷ 1422 R⁸ G¹⁸ 1423 R⁸ G¹⁹ 1424 R⁸ G²⁰ 1425 R⁹ G¹⁷ 1426 R⁹ G¹⁸ 1427 R⁹ G¹⁹ 1428 R⁹ G²⁰ 1429 R¹⁰ G¹⁷ 1430 R¹⁰ G¹⁸ 1431 R¹⁰ G¹⁹ 1432 R¹⁰ G²⁰ 1433 R¹¹ G¹⁷ 1434 R¹¹ G¹⁸ 1435 R¹¹ G¹⁹ 1436 R¹¹ G²⁰ 1437 R¹² G¹⁷ 1438 R¹² G¹⁸ 1439 R¹² G¹⁹ 1440 R¹² G²⁰ 1441 R¹³ G¹⁷ 1442 R¹³ G¹⁸ 1443 R¹³ G¹⁹ 1444 R¹³ G²⁰ 1445 R¹⁴ G¹⁷ 1446 R¹⁴ G¹⁸ 1447 R¹⁴ G¹⁹ 1448 R¹⁴ G²⁰ 1449 R¹⁵ G¹⁷ 1450 R¹⁵ G¹⁸ 1451 R¹⁵ G¹⁹ 1452 R¹⁵ G²⁰ 1453 R¹⁶ G¹⁷ 1454 R¹⁶ G¹⁸ 1455 R¹⁶ G¹⁹ 1456 R¹⁶ G²⁰ 1457 R¹⁷ G¹⁷ 1458 R¹⁷ G¹⁸ 1459 R¹⁷ G¹⁹ 1460 R¹⁷ G²⁰ 1461 R¹⁸ G¹⁷ 1462 R¹⁸ G¹⁸ 1463 R¹⁸ G¹⁹ 1464 R¹⁸ G²⁰ 1465 R¹⁹ G¹⁷ 1466 R¹⁹ G¹⁸ 1467 R¹⁹ G¹⁹ 1468 R¹⁹ G²⁰ 1469 R²⁰ G¹⁷ 1470 R²⁰ G¹⁸ 1471 R²⁰ G¹⁹ 1472 R²⁰ G²⁰ 1473 R²¹ G¹⁷ 1474 R²¹ G¹⁸ 1475 R²¹ G¹⁹ 1476 R²¹ G²⁰ 1477 R²² G¹⁷ 1478 R²² G¹⁸ 1479 R²² G¹⁹ 1480 R²² G²⁰ 1481 R²³ G¹⁷ 1482 R²³ G¹⁸ 1483 R²³ G¹⁹ 1484 R²³ G²⁰ 1485 R²⁴ G¹⁷ 1486 R²⁴ G¹⁸ 1487 R²⁴ G¹⁹ 1488 R²⁴ G²⁰ 1489 R²⁵ G¹⁷ 1490 R²⁵ G¹⁸ 1491 R²⁵ G¹⁹ 1492 R²⁵ G²⁰ 1493 R²⁶ G¹⁷ 1494 R²⁶ G¹⁸ 1495 R²⁶ G¹⁹ 1496 R²⁶ G²⁰ 1497 R²⁷ G¹⁷ 1498 R²⁷ G¹⁸ 1499 R²⁷ G¹⁹ 1500 R²⁷ G²⁰ 1501 R²⁸ G¹⁷ 1502 R²⁸ G¹⁸ 1503 R²⁸ G¹⁹ 1504 R²⁸ G²⁰ 1505 R²⁹ G¹⁷ 1506 R²⁹ G¹⁸ 1507 R²⁹ G¹⁹ 1508 R²⁹ G²⁰ 1509 R³⁰ G¹⁷ 1510 R³⁰ G¹⁸ 1511 R³⁰ G¹⁹ 1512 R³⁰ G²⁰ 1513 R³¹ G¹⁷ 1514 R³¹ G¹⁸ 1515 R³¹ G¹⁹ 1516 R³¹ G²⁰ 1517 R³² G¹⁷ 1518 R³² G¹⁸ 1519 R³² G¹⁹ 1520 R³² G²⁰ 1521 R³³ G¹⁷ 1522 R³³ G¹⁸ 1523 R³³ G¹⁹ 1524 R³³ G²⁰ 1525 R³⁴ G¹⁷ 1526 R³⁴ G¹⁸ 1527 R³⁴ G¹⁹ 1528 R³⁴ G²⁰ 1529 R³⁵ G¹⁷ 1530 R³⁵ G¹⁸ 1531 R³⁵ G¹⁹ 1532 R³⁵ G²⁰ 1533 R³⁶ G¹⁷ 1534 R³⁶ G¹⁸ 1535 R³⁶ G¹⁹ 1536 R³⁶ G²⁰ 1537 R³⁷ G¹⁷ 1538 R³⁷ G¹⁸ 1539 R³⁷ G¹⁹ 1540 R³⁷ G²⁰ 1541 R³⁸ G¹⁷ 1542 R³⁸ G¹⁸ 1543 R³⁸ G¹⁹ 1544 R³⁸ G²⁰ 1545 R³⁹ G¹⁷ 1546 R³⁹ G¹⁸ 1547 R³⁹ G¹⁹ 1548 R³⁹ G²⁰ 1549 R⁴⁰ G¹⁷ 1550 R⁴⁰ G¹⁸ 1551 R⁴⁰ G¹⁹ 1552 R⁴⁰ G²⁰ 1553 R⁴¹ G¹⁷ 1554 R⁴¹ G¹⁸ 1555 R⁴¹ G¹⁹ 1556 R⁴¹ G²⁰ 1557 R⁴² G¹⁷ 1558 R⁴² G¹⁸ 1559 R⁴² G¹⁹ 1560 R⁴² G²⁰ 1561 R⁴³ G¹⁷ 1562 R⁴³ G¹⁸ 1563 R⁴³ G¹⁹ 1564 R⁴³ G²⁰ 1565 R⁴⁴ G¹⁷ 1566 R⁴⁴ G¹⁸ 1567 R⁴⁴ G¹⁹ 1568 R⁴⁴ G²⁰ 1569 R⁴⁵ G¹⁷ 1570 R⁴⁵ G¹⁸ 1571 R⁴⁵ G¹⁹ 1572 R⁴⁵ G²⁰ 1573 R⁴⁶ G¹⁷ 1574 R⁴⁶ G¹⁸ 1575 R⁴⁶ G¹⁹ 1576 R⁴⁶ G²⁰ 1577 R⁴⁷ G¹⁷ 1578 R⁴⁷ G¹⁸ 1579 R⁴⁷ G¹⁹ 1580 R⁴⁷ G²⁰ 1581 R⁴⁸ G¹⁷ 1582 R⁴⁸ G¹⁸ 1583 R⁴⁸ G¹⁹ 1584 R⁴⁸ G²⁰ 1585 R⁴⁹ G¹⁷ 1586 R⁴⁹ G¹⁸ 1587 R⁴⁹ G¹⁹ 1588 R⁴⁹ G²⁰ 1589 R⁵⁰ G¹⁷ 1590 R⁵⁰ G¹⁸ 1591 R⁵⁰ G¹⁹ 1592 R⁵⁰ G²⁰ 1593 R⁵¹ G¹⁷ 1594 R⁵¹ G¹⁸ 1595 R⁵¹ G¹⁹ 1596 R⁵¹ G²⁰ 1597 R⁵² G¹⁷ 1598 R⁵² G¹⁸ 1599 R⁵² G¹⁹ 1600 R⁵² G²⁰ 1601 R⁵³ G¹⁷ 1602 R⁵³ G¹⁸ 1603 R⁵³ G¹⁹ 1604 R⁵³ G²⁰ 1605 R⁵⁴ G¹⁷ 1606 R⁵⁴ G¹⁸ 1607 R⁵⁴ G¹⁹ 1608 R⁵⁴ G²⁰ 1609 R⁵⁵ G¹⁷ 1610 R⁵⁵ G¹⁸ 1611 R⁵⁵ G¹⁹ 1612 R⁵⁵ G²⁰ 1613 R⁵⁶ G¹⁷ 1614 R⁵⁶ G¹⁸ 1615 R⁵⁶ G¹⁹ 1616 R⁵⁶ G²⁰ 1617 R⁵⁷ G¹⁷ 1618 R⁵⁷ G¹⁸ 1619 R⁵⁷ G¹⁹ 1620 R⁵⁷ G²⁰ 1621 R⁵⁸ G¹⁷ 1622 R⁵⁸ G¹⁸ 1623 R⁵⁸ G¹⁹ 1624 R⁵⁸ G²⁰ 1625 R⁵⁹ G¹⁷ 1626 R⁵⁹ G¹⁸ 1627 R⁵⁹ G¹⁹ 1628 R⁵⁹ G²⁰ 1629 R⁶⁰ G¹⁷ 1630 R⁶⁰ G¹⁸ 1631 R⁶⁰ G¹⁹ 1632 R⁶⁰ G²⁰ 1633 R⁶¹ G¹⁷ 1634 R⁶¹ G¹⁸ 1635 R⁶¹ G¹⁹ 1636 R⁶¹ G²⁰ 1637 R⁶² G¹⁷ 1638 R⁶² G¹⁸ 1639 R⁶² G¹⁹ 1640 R⁶² G²⁰ 1641 R⁶³ G¹⁷ 1642 R⁶³ G¹⁸ 1643 R⁶³ G¹⁹ 1644 R⁶³ G²⁰ 1645 R⁶⁴ G¹⁷ 1646 R⁶⁴ G¹⁸ 1647 R⁶⁴ G¹⁹ 1648 R⁶⁴ G²⁰ 1649 R⁶⁵ G¹⁷ 1650 R⁶⁵ G¹⁸ 1651 R⁶⁵ G¹⁹ 1652 R⁶⁵ G²⁰ 1653 R⁶⁶ G¹⁷ 1654 R⁶⁶ G¹⁸ 1655 R⁶⁶ G¹⁹ 1656 R⁶⁶ G²⁰ 1657 R⁶⁷ G¹⁷ 1658 R⁶⁷ G¹⁸ 1659 R⁶⁷ G¹⁹ 1660 R⁶⁷ G²⁰ 1661 R⁶⁸ G¹⁷ 1662 R⁶⁸ G¹⁸ 1663 R⁶⁸ G¹⁹ 1664 R⁶⁸ G²⁰ 1665 R⁶⁹ G¹⁷ 1666 R⁶⁹ G¹⁸ 1667 R⁶⁹ G¹⁹ 1668 R⁶⁹ G²⁰ 1669 R⁷⁰ G¹⁷ 1670 R⁷⁰ G¹⁸ 1671 R⁷⁰ G¹⁹ 1672 R⁷⁰ G²⁰ 1673 R⁷¹ G¹⁷ 1674 R⁷¹ G¹⁸ 1675 R⁷¹ G¹⁹ 1676 R⁷¹ G²⁰ 1677 R⁷² G¹⁷ 1678 R⁷² G¹⁸ 1679 R⁷² G¹⁹ 1680 R⁷² G²⁰ 1681 R⁷³ G¹⁷ 1682 R⁷³ G¹⁸ 1683 R⁷³ G¹⁹ 1684 R⁷³ G²⁰ 1685 R⁷⁴ G¹⁷ 1686 R⁷⁴ G¹⁸ 1687 R⁷⁴ G¹⁹ 1688 R⁷⁴ G²⁰ 1689 R⁷⁵ G¹⁷ 1690 R⁷⁵ G¹⁸ 1691 R⁷⁵ G¹⁹ 1692 R⁷⁵ G²⁰ 1693 R⁷⁶ G¹⁷ 1694 R⁷⁶ G¹⁸ 1695 R⁷⁶ G¹⁹ 1696 R⁷⁶ G²⁰ 1697 R⁷⁷ G¹⁷ 1698 R⁷⁷ G¹⁸ 1699 R⁷⁷ G¹⁹ 1700 R⁷⁷ G²⁰ 1701 R⁷⁸ G¹⁷ 1702 R⁷⁸ G¹⁸ 1703 R⁷⁸ G¹⁹ 1704 R⁷⁸ G²⁰ 1705 R⁷⁹ G¹⁷ 1706 R⁷⁹ G¹⁸ 1707 R⁷⁹ G¹⁹ 1708 R⁷⁹ G²⁰ 1709 R⁸⁰ G¹⁷ 1710 R⁸⁰ G¹⁸ 1711 R⁸⁰ G¹⁹ 1712 R⁸⁰ G²⁰ 1713 R⁸¹ G¹⁷ 1714 R⁸¹ G¹⁸ 1715 R⁸¹ G¹⁹ 1716 R⁸¹ G²⁰ 1717 R⁸² G¹⁷ 1718 R⁸² G¹⁸ 1719 R⁸² G¹⁹ 1720 R⁸² G²⁰ 1721 R⁸³ G¹⁷ 1722 R⁸³ G¹⁸ 1723 R⁸³ G¹⁹ 1724 R⁸³ G²⁰ 1725 R⁸⁴ G¹⁷ 1726 R⁸⁴ G¹⁸ 1727 R⁸⁴ G¹⁹ 1728 R⁸⁴ G²⁰ 1729 R⁸⁵ G¹⁷ 1730 R⁸⁵ G¹⁸ 1731 R⁸⁵ G¹⁹ 1732 R⁸⁵ G²⁰ 1733 R⁸⁶ G¹⁷ 1734 R⁸⁶ G¹⁸ 1735 R⁸⁶ G¹⁹ 1736 R⁸⁶ G²⁰ 1737 R⁸⁷ G¹⁷ 1738 R⁸⁷ G¹⁸ 1739 R⁸⁷ G¹⁹ 1740 R⁸⁷ G²⁰ 1741 R¹ G²¹ 1742 R¹ G²² 1743 R¹ G²³ 1744 R¹ G²⁴ 1745 R² G²¹ 1746 R² G²² 1747 R² G²³ 1748 R² G²⁴ 1749 R³ G²¹ 1750 R³ G²² 1751 R³ G²³ 1752 R³ G²⁴ 1753 R⁴ G²¹ 1754 R⁴ G²² 1755 R⁴ G²³ 1756 R⁴ G²⁴ 1757 R⁵ G²¹ 1758 R⁵ G²² 1759 R⁵ G²³ 1760 R⁵ G²⁴ 1761 R⁶ G²¹ 1762 R⁶ G²² 1763 R⁶ G²³ 1764 R⁶ G²⁴ 1765 R⁷ G²¹ 1766 R⁷ G²² 1767 R⁷ G²³ 1768 R⁷ G²⁴ 1769 R⁸ G²¹ 1770 R⁸ G²² 1771 R⁸ G²³ 1772 R⁸ G²⁴ 1773 R⁹ G²¹ 1774 R⁹ G²² 1775 R⁹ G²³ 1776 R⁹ G²⁴ 1777 R¹⁰ G²¹ 1778 R¹⁰ G²² 1779 R¹⁰ G²³ 1780 R¹⁰ G²⁴ 1781 R¹¹ G²¹ 1782 R¹¹ G²² 1783 R¹¹ G²³ 1784 R¹¹ G²⁴ 1785 R¹² G²¹ 1786 R¹² G²² 1787 R¹² G²³ 1788 R¹² G²⁴ 1789 R¹³ G²¹ 1790 R¹³ G²² 1791 R¹³ G²³ 1792 R¹³ G²⁴ 1793 R¹⁴ G²¹ 1794 R¹⁴ G²² 1795 R¹⁴ G²³ 1796 R¹⁴ G²⁴ 1797 R¹⁵ G²¹ 1798 R¹⁵ G²² 1799 R¹⁵ G²³ 1800 R¹⁵ G²⁴ 1801 R¹⁶ G²¹ 1802 R¹⁶ G²² 1803 R¹⁶ G²³ 1804 R¹⁶ G²⁴ 1805 R¹⁷ G²¹ 1806 R¹⁷ G²² 1807 R¹⁷ G²³ 1808 R¹⁷ G²⁴ 1809 R¹⁸ G²¹ 1810 R¹⁸ G²² 1811 R¹⁸ G²³ 1812 R¹⁸ G²⁴ 1813 R¹⁹ G²¹ 1814 R¹⁹ G²² 1815 R¹⁹ G²³ 1816 R¹⁹ G²⁴ 1817 R²⁰ G²¹ 1818 R²⁰ G²² 1819 R²⁰ G²³ 1820 R²⁰ G²⁴ 1821 R²¹ G²¹ 1822 R²¹ G²² 1823 R²¹ G²³ 1824 R²¹ G²⁴ 1825 R²² G²¹ 1826 R²² G²² 1827 R²² G²³ 1828 R²² G²⁴ 1829 R²³ G²¹ 1830 R²³ G²² 1831 R²³ G²³ 1832 R²³ G²⁴ 1833 R²⁴ G²¹ 1834 R²⁴ G²² 1835 R²⁴ G²³ 1836 R²⁴ G²⁴ 1837 R²⁵ G²¹ 1838 R²⁵ G²² 1839 R²⁵ G²³ 1840 R²⁵ G²⁴ 1841 R²⁶ G²¹ 1842 R²⁶ G²² 1843 R²⁶ G²³ 1844 R²⁶ G²⁴ 1845 R²⁷ G²¹ 1846 R²⁷ G²² 1847 R²⁷ G²³ 1848 R²⁷ G²⁴ 1849 R²⁸ G²¹ 1850 R²⁸ G²² 1851 R²⁸ G²³ 1852 R²⁸ G²⁴ 1853 R²⁹ G²¹ 1854 R²⁹ G²² 1855 R²⁹ G²³ 1856 R²⁹ G²⁴ 1857 R³⁰ G²¹ 1858 R³⁰ G²² 1859 R³⁰ G²³ 1860 R³⁰ G²⁴ 1861 R³¹ G²¹ 1862 R³¹ G²² 1863 R³¹ G²³ 1864 R³¹ G²⁴ 1865 R³² G²¹ 1866 R³² G²² 1867 R³² G²³ 1868 R³² G²⁴ 1869 R³³ G²¹ 1870 R³³ G²² 1871 R³³ G²³ 1872 R³³ G²⁴ 1873 R³⁴ G²¹ 1874 R³⁴ G²² 1875 R³⁴ G²³ 1876 R³⁴ G²⁴ 1877 R³⁵ G²¹ 1878 R³⁵ G²² 1879 R³⁵ G²³ 1880 R³⁵ G²⁴ 1881 R³⁶ G²¹ 1882 R³⁶ G²² 1883 R³⁶ G²³ 1884 R³⁶ G²⁴ 1885 R³⁷ G²¹ 1886 R³⁷ G²² 1887 R³⁷ G²³ 1888 R³⁷ G²⁴ 1889 R³⁸ G²¹ 1890 R³⁸ G²² 1891 R³⁸ G²³ 1892 R³⁸ G²⁴ 1893 R³⁹ G²¹ 1894 R³⁹ G²² 1895 R³⁹ G²³ 1896 R³⁹ G²⁴ 1897 R⁴⁰ G²¹ 1898 R⁴⁰ G²² 1899 R⁴⁰ G²³ 1900 R⁴⁰ G²⁴ 1901 R⁴¹ G²¹ 1902 R⁴¹ G²² 1903 R⁴¹ G²³ 1904 R⁴¹ G²⁴ 1905 R⁴² G²¹ 1906 R⁴² G²² 1907 R⁴² G²³ 1908 R⁴² G²⁴ 1909 R⁴³ G²¹ 1910 R⁴³ G²² 1911 R⁴³ G²³ 1912 R⁴³ G²⁴ 1913 R⁴⁴ G²¹ 1914 R⁴⁴ G²² 1915 R⁴⁴ G²³ 1916 R⁴⁴ G²⁴ 1917 R⁴⁵ G²¹ 1918 R⁴⁵ G²² 1919 R⁴⁵ G²³ 1920 R⁴⁵ G²⁴ 1921 R⁴⁶ G²¹ 1922 R⁴⁶ G²² 1923 R⁴⁶ G²³ 1924 R⁴⁶ G²⁴ 1925 R⁴⁷ G²¹ 1926 R⁴⁷ G²² 1927 R⁴⁷ G²³ 1928 R⁴⁷ G²⁴ 1929 R⁴⁸ G²¹ 1930 R⁴⁸ G²² 1931 R⁴⁸ G²³ 1932 R⁴⁸ G²⁴ 1933 R⁴⁹ G²¹ 1934 R⁴⁹ G²² 1935 R⁴⁹ G²³ 1936 R⁴⁹ G²⁴ 1937 R⁵⁰ G²¹ 1938 R⁵⁰ G²² 1939 R⁵⁰ G²³ 1940 R⁵⁰ G²⁴ 1941 R⁵¹ G²¹ 1942 R⁵¹ G²² 1943 R⁵¹ G²³ 1944 R⁵¹ G²⁴ 1945 R⁵² G²¹ 1946 R⁵² G²² 1947 R⁵² G²³ 1948 R⁵² G²⁴ 1949 R⁵³ G²¹ 1950 R⁵³ G²² 1951 R⁵³ G²³ 1952 R⁵³ G²⁴ 1953 R⁵⁴ G²¹ 1954 R⁵⁴ G²² 1955 R⁵⁴ G²³ 1956 R⁵⁴ G²⁴ 1957 R⁵⁵ G²¹ 1958 R⁵⁵ G²² 1959 R⁵⁵ G²³ 1960 R⁵⁵ G²⁴ 1961 R⁵⁶ G²¹ 1962 R⁵⁶ G²² 1963 R⁵⁶ G²³ 1964 R⁵⁶ G²⁴ 1965 R⁵⁷ G²¹ 1966 R⁵⁷ G²² 1967 R⁵⁷ G²³ 1968 R⁵⁷ G²⁴ 1969 R⁵⁸ G²¹ 1970 R⁵⁸ G²² 1971 R⁵⁸ G²³ 1972 R⁵⁸ G²⁴ 1973 R⁵⁹ G²¹ 1974 R⁵⁹ G²² 1975 R⁵⁹ G²³ 1976 R⁵⁹ G²⁴ 1977 R⁶⁰ G²¹ 1978 R⁶⁰ G²² 1979 R⁶⁰ G²³ 1980 R⁶⁰ G²⁴ 1981 R⁶¹ G²¹ 1982 R⁶¹ G²² 1983 R⁶¹ G²³ 1984 R⁶¹ G²⁴ 1985 R⁶² G²¹ 1986 R⁶² G²² 1987 R⁶² G²³ 1988 R⁶² G²⁴ 1989 R⁶³ G²¹ 1990 R⁶³ G²² 1991 R⁶³ G²³ 1992 R⁶³ G²⁴ 1993 R⁶⁴ G²¹ 1994 R⁶⁴ G²² 1995 R⁶⁴ G²³ 1996 R⁶⁴ G²⁴ 1997 R⁶⁵ G²¹ 1998 R⁶⁵ G²² 1999 R⁶⁵ G²³ 2000 R⁶⁵ G²⁴ 2001 R⁶⁶ G²¹ 2002 R⁶⁶ G²² 2003 R⁶⁶ G²³ 2004 R⁶⁶ G²⁴ 2005 R⁶⁷ G²¹ 2006 R⁶⁷ G²² 2007 R⁶⁷ G²³ 2008 R⁶⁷ G²⁴ 2009 R⁶⁸ G²¹ 2010 R⁶⁸ G²² 2011 R⁶⁸ G²³ 2012 R⁶⁸ G²⁴ 2013 R⁶⁹ G²¹ 2014 R⁶⁹ G²² 2015 R⁶⁹ G²³ 2016 R⁶⁹ G²⁴ 2017 R⁷⁰ G²¹ 2018 R⁷⁰ G²² 2019 R⁷⁰ G²³ 2020 R⁷⁰ G²⁴ 2021 R⁷¹ G²¹ 2022 R⁷¹ G²² 2023 R⁷¹ G²³ 2024 R⁷¹ G²⁴ 2025 R⁷² G²¹ 2026 R⁷² G²² 2027 R⁷² G²³ 2028 R⁷² G²⁴ 2029 R⁷³ G²¹ 2030 R⁷³ G²² 2031 R⁷³ G²³ 2032 R⁷³ G²⁴ 2033 R⁷⁴ G²¹ 2034 R⁷⁴ G²² 2035 R⁷⁴ G²³ 2036 R⁷⁴ G²⁴ 2037 R⁷⁵ G²¹ 2038 R⁷⁵ G²² 2039 R⁷⁵ G²³ 2040 R⁷⁵ G²⁴ 2041 R⁷⁶ G²¹ 2042 R⁷⁶ G²² 2043 R⁷⁶ G²³ 2044 R⁷⁶ G²⁴ 2045 R⁷⁷ G²¹ 2046 R⁷⁷ G²² 2047 R⁷⁷ G²³ 2048 R⁷⁷ G²⁴ 2049 R⁷⁸ G²¹ 2050 R⁷⁸ G²² 2051 R⁷⁸ G²³ 2052 R⁷⁸ G²⁴ 2053 R⁷⁹ G²¹ 2054 R⁷⁹ G²² 2055 R⁷⁹ G²³ 2056 R⁷⁹ G²⁴ 2057 R⁸⁰ G²¹ 2058 R⁸⁰ G²² 2059 R⁸⁰ G²³ 2060 R⁸⁰ G²⁴ 2061 R⁸¹ G²¹ 2062 R⁸¹ G²² 2063 R⁸¹ G²³ 2064 R⁸¹ G²⁴ 2065 R⁸² G²¹ 2066 R⁸² G²² 2067 R⁸² G²³ 2068 R⁸² G²⁴ 2069 R⁸³ G²¹ 2070 R⁸³ G²² 2071 R⁸³ G²³ 2072 R⁸³ G²⁴ 2073 R⁸⁴ G²¹ 2074 R⁸⁴ G²² 2075 R⁸⁴ G²³ 2076 R⁸⁴ G²⁴ 2077 R⁸⁵ G²¹ 2078 R⁸⁵ G²² 2079 R⁸⁵ G²³ 2080 R⁸⁵ G²⁴ 2081 R⁸⁶ G²¹ 2082 R⁸⁶ G²² 2083 R⁸⁶ G²³ 2084 R⁸⁶ G²⁴ 2085 R⁸⁷ G²¹ 2086 R⁸⁷ G²² 2087 R⁸⁷ G²³ 2088 R⁸⁷ G²⁴ 2089 R¹ G²⁵ 2090 R¹ G²⁶ 2091 R¹ G²⁷ 2092 R¹ G²⁸ 2093 R² G²⁵ 2094 R² G²⁶ 2095 R² G²⁷ 2096 R² G²⁸ 2097 R³ G²⁵ 2098 R³ G²⁶ 2099 R³ G²⁷ 2100 R³ G²⁸ 2101 R⁴ G²⁵ 2102 R⁴ G²⁶ 2103 R⁴ G²⁷ 2104 R⁴ G²⁸ 2105 R⁵ G²⁵ 2106 R⁵ G²⁶ 2107 R⁵ G²⁷ 2108 R⁵ G²⁸ 2109 R⁶ G²⁵ 2110 R⁶ G²⁶ 2111 R⁶ G²⁷ 2112 R⁶ G²⁸ 2113 R⁷ G²⁵ 2114 R⁷ G²⁶ 2115 R⁷ G²⁷ 2116 R⁷ G²⁸ 2117 R⁸ G²⁵ 2118 R⁸ G²⁶ 2119 R⁸ G²⁷ 2120 R⁸ G²⁸ 2121 R⁹ G²⁵ 2122 R⁹ G²⁶ 2123 R⁹ G²⁷ 2124 R⁹ G²⁸ 2125 R¹⁰ G²⁵ 2126 R¹⁰ G²⁶ 2127 R¹⁰ G²⁷ 2128 R¹⁰ G²⁸ 2129 R¹¹ G²⁵ 2130 R¹¹ G²⁶ 2131 R¹¹ G²⁷ 2132 R¹¹ G²⁸ 2133 R¹² G²⁵ 2134 R¹² G²⁶ 2135 R¹² G²⁷ 2136 R¹² G²⁸ 2137 R¹³ G²⁵ 2138 R¹³ G²⁶ 2139 R¹³ G²⁷ 2140 R¹³ G²⁸ 2141 R¹⁴ G²⁵ 2142 R¹⁴ G²⁶ 2143 R¹⁴ G²⁷ 2144 R¹⁴ G²⁸ 2145 R¹⁵ G²⁵ 2146 R¹⁵ G²⁶ 2147 R¹⁵ G²⁷ 2148 R¹⁵ G²⁸ 2149 R¹⁶ G²⁵ 2150 R¹⁶ G²⁶ 2151 R¹⁶ G²⁷ 2152 R¹⁶ G²⁸ 2153 R¹⁷ G²⁵ 2154 R¹⁷ G²⁶ 2155 R¹⁷ G²⁷ 2156 R¹⁷ G²⁸ 2157 R¹⁸ G²⁵ 2158 R¹⁸ G²⁶ 2159 R¹⁸ G²⁷ 2160 R¹⁸ G²⁸ 2161 R¹⁹ G²⁵ 2162 R¹⁹ G²⁶ 2163 R¹⁹ G²⁷ 2164 R¹⁹ G²⁸ 2165 R²⁰ G²⁵ 2166 R²⁰ G²⁶ 2167 R²⁰ G²⁷ 2168 R²⁰ G²⁸ 2169 R²¹ G²⁵ 2170 R²¹ G²⁶ 2171 R²¹ G²⁷ 2172 R²¹ G²⁸ 2173 R²² G²⁵ 2174 R²² G²⁶ 2175 R²² G²⁷ 2176 R²² G²⁸ 2177 R²³ G²⁵ 2178 R²³ G²⁶ 2179 R²³ G²⁷ 2180 R²³ G²⁸ 2181 R²⁴ G²⁵ 2182 R²⁴ G²⁶ 2183 R²⁴ G²⁷ 2184 R²⁴ G²⁸ 2185 R²⁵ G²⁵ 2186 R²⁵ G²⁶ 2187 R²⁵ G²⁷ 2188 R²⁵ G²⁸ 2189 R²⁶ G²⁵ 2190 R²⁶ G²⁶ 2191 R²⁶ G²⁷ 2192 R²⁶ G²⁸ 2193 R²⁷ G²⁵ 2194 R²⁷ G²⁶ 2195 R²⁷ G²⁷ 2196 R²⁷ G²⁸ 2197 R²⁸ G²⁵ 2198 R²⁸ G²⁶ 2199 R²⁸ G²⁷ 2200 R²⁸ G²⁸ 2201 R²⁹ G²⁵ 2202 R²⁹ G²⁶ 2203 R²⁹ G²⁷ 2204 R²⁹ G²⁸ 2205 R³⁰ G²⁵ 2206 R³⁰ G²⁶ 2207 R³⁰ G²⁷ 2208 R³⁰ G²⁸ 2209 R³¹ G²⁵ 2210 R³¹ G²⁶ 2211 R³¹ G²⁷ 2212 R³¹ G²⁸ 2213 R³² G²⁵ 2214 R³² G²⁶ 2215 R³² G²⁷ 2216 R³² G²⁸ 2217 R³³ G²⁵ 2218 R³³ G²⁶ 2219 R³³ G²⁷ 2220 R³³ G²⁸ 2221 R³⁴ G²⁵ 2222 R³⁴ G²⁶ 2223 R³⁴ G²⁷ 2224 R³⁴ G²⁸ 2225 R³⁵ G²⁵ 2226 R³⁵ G²⁶ 2227 R³⁵ G²⁷ 2228 R³⁵ G²⁸ 2229 R³⁶ G²⁵ 2230 R³⁶ G²⁶ 2231 R³⁶ G²⁷ 2232 R³⁶ G²⁸ 2233 R³⁷ G²⁵ 2234 R³⁷ G²⁶ 2235 R³⁷ G²⁷ 2236 R³⁷ G²⁸ 2237 R³⁸ G²⁵ 2238 R³⁸ G²⁶ 2239 R³⁸ G²⁷ 2240 R³⁸ G²⁸ 2241 R³⁹ G²⁵ 2242 R³⁹ G²⁶ 2243 R³⁹ G²⁷ 2244 R³⁹ G²⁸ 2245 R⁴⁰ G²⁵ 2246 R⁴⁰ G²⁶ 2247 R⁴⁰ G²⁷ 2248 R⁴⁰ G²⁸ 2249 R⁴¹ G²⁵ 2250 R⁴¹ G²⁶ 2251 R⁴¹ G²⁷ 2252 R⁴¹ G²⁸ 2253 R⁴² G²⁵ 2254 R⁴² G²⁶ 2255 R⁴² G²⁷ 2256 R⁴² G²⁸ 2257 R⁴³ G²⁵ 2258 R⁴³ G²⁶ 2259 R⁴³ G²⁷ 2260 R⁴³ G²⁸ 2261 R⁴⁴ G²⁵ 2262 R⁴⁴ G²⁶ 2263 R⁴⁴ G²⁷ 2264 R⁴⁴ G²⁸ 2265 R⁴⁵ G²⁵ 2266 R⁴⁵ G²⁶ 2267 R⁴⁵ G²⁷ 2268 R⁴⁵ G²⁸ 2269 R⁴⁶ G²⁵ 2270 R⁴⁶ G²⁶ 2271 R⁴⁶ G²⁷ 2272 R⁴⁶ G²⁸ 2273 R⁴⁷ G²⁵ 2274 R⁴⁷ G²⁶ 2275 R⁴⁷ G²⁷ 2276 R⁴⁷ G²⁸ 2277 R⁴⁸ G²⁵ 2278 R⁴⁸ G²⁶ 2279 R⁴⁸ G²⁷ 2280 R⁴⁸ G²⁸ 2281 R⁴⁹ G²⁵ 2282 R⁴⁹ G²⁶ 2283 R⁴⁹ G²⁷ 2284 R⁴⁹ G²⁸ 2285 R⁵⁰ G²⁵ 2286 R⁵⁰ G²⁶ 2287 R⁵⁰ G²⁷ 2288 R⁵⁰ G²⁸ 2289 R⁵¹ G²⁵ 2290 R⁵¹ G²⁶ 2291 R⁵¹ G²⁷ 2292 R⁵¹ G²⁸ 2293 R⁵² G²⁵ 2294 R⁵² G²⁶ 2295 R⁵² G²⁷ 2296 R⁵² G²⁸ 2297 R⁵³ G²⁵ 2298 R⁵³ G²⁶ 2299 R⁵³ G²⁷ 2300 R⁵³ G²⁸ 2301 R⁵⁴ G²⁵ 2302 R⁵⁴ G²⁶ 2303 R⁵⁴ G²⁷ 2304 R⁵⁴ G²⁸ 2305 R⁵⁵ G²⁵ 2306 R⁵⁵ G²⁶ 2307 R⁵⁵ G²⁷ 2308 R⁵⁵ G²⁸ 2309 R⁵⁶ G²⁵ 2310 R⁵⁶ G²⁶ 2311 R⁵⁶ G²⁷ 2312 R⁵⁶ G²⁸ 2313 R⁵⁷ G²⁵ 2314 R⁵⁷ G²⁶ 2315 R⁵⁷ G²⁷ 2316 R⁵⁷ G²⁸ 2317 R⁵⁸ G²⁵ 2318 R⁵⁸ G²⁶ 2319 R⁵⁸ G²⁷ 2320 R⁵⁸ G²⁸ 2321 R⁵⁹ G²⁵ 2322 R⁵⁹ G²⁶ 2323 R⁵⁹ G²⁷ 2324 R⁵⁹ G²⁸ 2325 R⁶⁰ G²⁵ 2326 R⁶⁰ G²⁶ 2327 R⁶⁰ G²⁷ 2328 R⁶⁰ G²⁸ 2329 R⁶¹ G²⁵ 2330 R⁶¹ G²⁶ 2331 R⁶¹ G²⁷ 2332 R⁶¹ G²⁸ 2333 R⁶² G²⁵ 2334 R⁶² G²⁶ 2335 R⁶² G²⁷ 2336 R⁶² G²⁸ 2337 R⁶³ G²⁵ 2338 R⁶³ G²⁶ 2339 R⁶³ G²⁷ 2340 R⁶³ G²⁸ 2341 R⁶⁴ G²⁵ 2342 R⁶⁴ G²⁶ 2343 R⁶⁴ G²⁷ 2344 R⁶⁴ G²⁸ 2345 R⁶⁵ G²⁵ 2346 R⁶⁵ G²⁶ 2347 R⁶⁵ G²⁷ 2348 R⁶⁵ G²⁸ 2349 R⁶⁶ G²⁵ 2350 R⁶⁶ G²⁶ 2351 R⁶⁶ G²⁷ 2352 R⁶⁶ G²⁸ 2353 R⁶⁷ G²⁵ 2354 R⁶⁷ G²⁶ 2355 R⁶⁷ G²⁷ 2356 R⁶⁷ G²⁸ 2357 R⁶⁸ G²⁵ 2358 R⁶⁸ G²⁶ 2359 R⁶⁸ G²⁷ 2360 R⁶⁸ G²⁸ 2361 R⁶⁹ G²⁵ 2362 R⁶⁹ G²⁶ 2363 R⁶⁹ G²⁷ 2364 R⁶⁹ G²⁸ 2365 R⁷⁰ G²⁵ 2366 R⁷⁰ G²⁶ 2367 R⁷⁰ G²⁷ 2368 R⁷⁰ G²⁸ 2369 R⁷¹ G²⁵ 2370 R⁷¹ G²⁶ 2371 R⁷¹ G²⁷ 2372 R⁷¹ G²⁸ 2373 R⁷² G²⁵ 2374 R⁷² G²⁶ 2375 R⁷² G²⁷ 2376 R⁷² G²⁸ 2377 R⁷³ G²⁵ 2378 R⁷³ G²⁶ 2379 R⁷³ G²⁷ 2380 R⁷³ G²⁸ 2381 R⁷⁴ G²⁵ 2382 R⁷⁴ G²⁶ 2383 R⁷⁴ G²⁷ 2384 R⁷⁴ G²⁸ 2385 R⁷⁵ G²⁵ 2386 R⁷⁵ G²⁶ 2387 R⁷⁵ G²⁷ 2388 R⁷⁵ G²⁸ 2389 R⁷⁶ G²⁵ 2390 R⁷⁶ G²⁶ 2391 R⁷⁶ G²⁷ 2392 R⁷⁶ G²⁸ 2393 R⁷⁷ G²⁵ 2394 R⁷⁷ G²⁶ 2395 R⁷⁷ G²⁷ 2396 R⁷⁷ G²⁸ 2397 R⁷⁸ G²⁵ 2398 R⁷⁸ G²⁶ 2399 R⁷⁸ G²⁷ 2400 R⁷⁸ G²⁸ 2401 R⁷⁹ G²⁵ 2402 R⁷⁹ G²⁶ 2403 R⁷⁹ G²⁷ 2404 R⁷⁹ G²⁸ 2405 R⁸⁰ G²⁵ 2406 R⁸⁰ G²⁶ 2407 R⁸⁰ G²⁷ 2408 R⁸⁰ G²⁸ 2409 R⁸¹ G²⁵ 2410 R⁸¹ G²⁶ 2411 R⁸¹ G²⁷ 2412 R⁸¹ G²⁸ 2413 R⁸² G²⁵ 2414 R⁸² G²⁶ 2415 R⁸² G²⁷ 2416 R⁸² G²⁸ 2417 R⁸³ G²⁵ 2418 R⁸³ G²⁶ 2419 R⁸³ G²⁷ 2420 R⁸³ G²⁸ 2421 R⁸⁴ G²⁵ 2422 R⁸⁴ G²⁶ 2423 R⁸⁴ G²⁷ 2424 R⁸⁴ G²⁸ 2425 R⁸⁵ G²⁵ 2426 R⁸⁵ G²⁶ 2427 R⁸⁵ G²⁷ 2428 R⁸⁵ G²⁸ 2429 R⁸⁶ G²⁵ 2430 R⁸⁶ G²⁶ 2431 R⁸⁶ G²⁷ 2432 R⁸⁶ G²⁸ 2433 R⁸⁷ G²⁵ 2434 R⁸⁷ G²⁶ 2435 R⁸⁷ G²⁷ 2436 R⁸⁷ G²⁸ 2437 R¹ G²⁹ 2438 R¹ G³⁰ 2439 R¹ G³¹ 2440 R¹ G³² 2441 R² G²⁹ 2442 R² G³⁰ 2443 R² G³¹ 2444 R² G³² 2445 R³ G²⁹ 2446 R³ G³⁰ 2447 R³ G³¹ 2448 R³ G³² 2449 R⁴ G²⁹ 2450 R⁴ G³⁰ 2451 R⁴ G³¹ 2452 R⁴ G³² 2453 R⁵ G²⁹ 2454 R⁵ G³⁰ 2455 R⁵ G³¹ 2456 R⁵ G³² 2457 R⁶ G²⁹ 2458 R⁶ G³⁰ 2459 R⁶ G³¹ 2460 R⁶ G³² 2461 R⁷ G²⁹ 2462 R⁷ G³⁰ 2463 R⁷ G³¹ 2464 R⁷ G³² 2465 R⁸ G²⁹ 2466 R⁸ G³⁰ 2467 R⁸ G³¹ 2468 R⁸ G³² 2469 R⁹ G²⁹ 2470 R⁹ G³⁰ 2471 R⁹ G³¹ 2472 R⁹ G³² 2473 R¹⁰ G²⁹ 2474 R¹⁰ G³⁰ 2475 R¹⁰ G³¹ 2476 R¹⁰ G³² 2477 R¹¹ G²⁹ 2478 R¹¹ G³⁰ 2479 R¹¹ G³¹ 2480 R¹¹ G³² 2481 R¹² G²⁹ 2482 R¹² G³⁰ 2483 R¹² G³¹ 2484 R¹² G³² 2485 R¹³ G²⁹ 2486 R¹³ G³⁰ 2487 R¹³ G³¹ 2488 R¹³ G³² 2489 R¹⁴ G²⁹ 2490 R¹⁴ G³⁰ 2491 R¹⁴ G³¹ 2492 R¹⁴ G³² 2493 R¹⁵ G²⁹ 2494 R¹⁵ G³⁰ 2495 R¹⁵ G³¹ 2496 R¹⁵ G³² 2497 R¹⁶ G²⁹ 2498 R¹⁶ G³⁰ 2499 R¹⁶ G³¹ 2500 R¹⁶ G³² 2501 R¹⁷ G²⁹ 2502 R¹⁷ G³⁰ 2503 R¹⁷ G³¹ 2504 R¹⁷ G³² 2505 R¹⁸ G²⁹ 2506 R¹⁸ G³⁰ 2507 R¹⁸ G³¹ 2508 R¹⁸ G³² 2509 R¹⁹ G²⁹ 2510 R¹⁹ G³⁰ 2511 R¹⁹ G³¹ 2512 R¹⁹ G³² 2513 R²⁰ G²⁹ 2514 R²⁰ G³⁰ 2515 R²⁰ G³¹ 2516 R²⁰ G³² 2517 R²¹ G²⁹ 2518 R²¹ G³⁰ 2519 R²¹ G³¹ 2520 R²¹ G³² 2521 R²² G²⁹ 2522 R²² G³⁰ 2523 R²² G³¹ 2524 R²² G³² 2525 R²³ G²⁹ 2526 R²³ G³⁰ 2527 R²³ G³¹ 2528 R²³ G³² 2529 R²⁴ G²⁹ 2530 R²⁴ G³⁰ 2531 R²⁴ G³¹ 2532 R²⁴ G³² 2533 R²⁵ G²⁹ 2534 R²⁵ G³⁰ 2535 R²⁵ G³¹ 2536 R²⁵ G³² 2537 R²⁶ G²⁹ 2538 R²⁶ G³⁰ 2539 R²⁶ G³¹ 2540 R²⁶ G³² 2541 R²⁷ G²⁹ 2542 R²⁷ G³⁰ 2543 R²⁷ G³¹ 2544 R²⁷ G³² 2545 R²⁸ G²⁹ 2546 R²⁸ G³⁰ 2547 R²⁸ G³¹ 2548 R²⁸ G³² 2549 R²⁹ G²⁹ 2550 R²⁹ G³⁰ 2551 R²⁹ G³¹ 2552 R²⁹ G³² 2553 R³⁰ G²⁹ 2554 R³⁰ G³⁰ 2555 R³⁰ G³¹ 2556 R³⁰ G³² 2557 R³¹ G²⁹ 2558 R³¹ G³⁰ 2559 R³¹ G³¹ 2560 R³¹ G³² 2561 R³² G²⁹ 2562 R³² G³⁰ 2563 R³² G³¹ 2564 R³² G³² 2565 R³³ G²⁹ 2566 R³³ G³⁰ 2567 R³³ G³¹ 2568 R³³ G³² 2569 R³⁴ G²⁹ 2570 R³⁴ G³⁰ 2571 R³⁴ G³¹ 2572 R³⁴ G³² 2573 R³⁵ G²⁹ 2574 R³⁵ G³⁰ 2575 R³⁵ G³¹ 2576 R³⁵ G³² 2577 R³⁶ G²⁹ 2578 R³⁶ G³⁰ 2579 R³⁶ G³¹ 2580 R³⁶ G³² 2581 R³⁷ G²⁹ 2582 R³⁷ G³⁰ 2583 R³⁷ G³¹ 2584 R³⁷ G³² 2585 R³⁸ G²⁹ 2586 R³⁸ G³⁰ 2587 R³⁸ G³¹ 2588 R³⁸ G³² 2589 R³⁹ G²⁹ 2590 R³⁹ G³⁰ 2591 R³⁹ G³¹ 2592 R³⁹ G³² 2593 R⁴⁰ G²⁹ 2594 R⁴⁰ G³⁰ 2595 R⁴⁰ G³¹ 2596 R⁴⁰ G³² 2597 R⁴¹ G²⁹ 2598 R⁴¹ G³⁰ 2599 R⁴¹ G³¹ 2600 R⁴¹ G³² 2601 R⁴² G²⁹ 2602 R⁴² G³⁰ 2603 R⁴² G³¹ 2604 R⁴² G³² 2605 R⁴³ G²⁹ 2606 R⁴³ G³⁰ 2607 R⁴³ G³¹ 2608 R⁴³ G³² 2609 R⁴⁴ G²⁹ 2610 R⁴⁴ G³⁰ 2611 R⁴⁴ G³¹ 2612 R⁴⁴ G³² 2613 R⁴⁵ G²⁹ 2614 R⁴⁵ G³⁰ 2615 R⁴⁵ G³¹ 2616 R⁴⁵ G³² 2617 R⁴⁶ G²⁹ 2618 R⁴⁶ G³⁰ 2619 R⁴⁶ G³¹ 2620 R⁴⁶ G³² 2621 R⁴⁷ G²⁹ 2622 R⁴⁷ G³⁰ 2623 R⁴⁷ G³¹ 2624 R⁴⁷ G³² 2625 R⁴⁸ G²⁹ 2626 R⁴⁸ G³⁰ 2627 R⁴⁸ G³¹ 2628 R⁴⁸ G³² 2629 R⁴⁹ G²⁹ 2630 R⁴⁹ G³⁰ 2631 R⁴⁹ G³¹ 2632 R⁴⁹ G³² 2633 R⁵⁰ G²⁹ 2634 R⁵⁰ G³⁰ 2635 R⁵⁰ G³¹ 2636 R⁵⁰ G³² 2637 R⁵¹ G²⁹ 2638 R⁵¹ G³⁰ 2639 R⁵¹ G³¹ 2640 R⁵¹ G³² 2641 R⁵² G²⁹ 2642 R⁵² G³⁰ 2643 R⁵² G³¹ 2644 R⁵² G³² 2645 R⁵³ G²⁹ 2646 R⁵³ G³⁰ 2647 R⁵³ G³¹ 2648 R⁵³ G³² 2649 R⁵⁴ G²⁹ 2650 R⁵⁴ G³⁰ 2651 R⁵⁴ G³¹ 2652 R⁵⁴ G³² 2653 R⁵⁵ G²⁹ 2654 R⁵⁵ G³⁰ 2655 R⁵⁵ G³¹ 2656 R⁵⁵ G³² 2657 R⁵⁶ G²⁹ 2658 R⁵⁶ G³⁰ 2659 R⁵⁶ G³¹ 2660 R⁵⁶ G³² 2661 R⁵⁷ G²⁹ 2662 R⁵⁷ G³⁰ 2663 R⁵⁷ G³¹ 2664 R⁵⁷ G³² 2665 R⁵⁸ G²⁹ 2666 R⁵⁸ G³⁰ 2667 R⁵⁸ G³¹ 2668 R⁵⁸ G³² 2669 R⁵⁹ G²⁹ 2670 R⁵⁹ G³⁰ 2671 R⁵⁹ G³¹ 2672 R⁵⁹ G³² 2673 R⁶⁰ G²⁹ 2674 R⁶⁰ G³⁰ 2675 R⁶⁰ G³¹ 2676 R⁶⁰ G³² 2677 R⁶¹ G²⁹ 2678 R⁶¹ G³⁰ 2679 R⁶¹ G³¹ 2680 R⁶¹ G³² 2681 R⁶² G²⁹ 2682 R⁶² G³⁰ 2683 R⁶² G³¹ 2684 R⁶² G³² 2685 R⁶³ G²⁹ 2686 R⁶³ G³⁰ 2687 R⁶³ G³¹ 2688 R⁶³ G³² 2689 R⁶⁴ G²⁹ 2690 R⁶⁴ G³⁰ 2691 R⁶⁴ G³¹ 2692 R⁶⁴ G³² 2693 R⁶⁵ G²⁹ 2694 R⁶⁵ G³⁰ 2695 R⁶⁵ G³¹ 2696 R⁶⁵ G³² 2697 R⁶⁶ G²⁹ 2698 R⁶⁶ G³⁰ 2699 R⁶⁶ G³¹ 2700 R⁶⁶ G³² 2701 R⁶⁷ G²⁹ 2702 R⁶⁷ G³⁰ 2703 R⁶⁷ G³¹ 2704 R⁶⁷ G³² 2705 R⁶⁸ G²⁹ 2706 R⁶⁸ G³⁰ 2707 R⁶⁸ G³¹ 2708 R⁶⁸ G³² 2709 R⁶⁹ G²⁹ 2710 R⁶⁹ G³⁰ 2711 R⁶⁹ G³¹ 2712 R⁶⁹ G³² 2713 R⁷⁰ G²⁹ 2714 R⁷⁰ G³⁰ 2715 R⁷⁰ G³¹ 2716 R⁷⁰ G³² 2717 R⁷¹ G²⁹ 2718 R⁷¹ G³⁰ 2719 R⁷¹ G³¹ 2720 R⁷¹ G³² 2721 R⁷² G²⁹ 2722 R⁷² G³⁰ 2723 R⁷² G³¹ 2724 R⁷² G³² 2725 R⁷³ G²⁹ 2726 R⁷³ G³⁰ 2727 R⁷³ G³¹ 2728 R⁷³ G³² 2729 R⁷⁴ G²⁹ 2730 R⁷⁴ G³⁰ 2731 R⁷⁴ G³¹ 2732 R⁷⁴ G³² 2733 R⁷⁵ G²⁹ 2734 R⁷⁵ G³⁰ 2735 R⁷⁵ G³¹ 2736 R⁷⁵ G³² 2737 R⁷⁶ G²⁹ 2738 R⁷⁶ G³⁰ 2739 R⁷⁶ G³¹ 2740 R⁷⁶ G³² 2741 R⁷⁷ G²⁹ 2742 R⁷⁷ G³⁰ 2743 R⁷⁷ G³¹ 2744 R⁷⁷ G³² 2745 R⁷⁸ G²⁹ 2746 R⁷⁸ G³⁰ 2747 R⁷⁸ G³¹ 2748 R⁷⁸ G³² 2749 R⁷⁹ G²⁹ 2750 R⁷⁹ G³⁰ 2751 R⁷⁹ G³¹ 2752 R⁷⁹ G³² 2753 R⁸⁰ G²⁹ 2754 R⁸⁰ G³⁰ 2755 R⁸⁰ G³¹ 2756 R⁸⁰ G³² 2757 R⁸¹ G²⁹ 2758 R⁸¹ G³⁰ 2759 R⁸¹ G³¹ 2760 R⁸¹ G³² 2761 R⁸² G²⁹ 2762 R⁸² G³⁰ 2763 R⁸² G³¹ 2764 R⁸² G³² 2765 R⁸³ G²⁹ 2766 R⁸³ G³⁰ 2767 R⁸³ G³¹ 2768 R⁸³ G³² 2769 R⁸⁴ G²⁹ 2770 R⁸⁴ G³⁰ 2771 R⁸⁴ G³¹ 2772 R⁸⁴ G³² 2773 R⁸⁵ G²⁹ 2774 R⁸⁵ G³⁰ 2775 R⁸⁵ G³¹ 2776 R⁸⁵ G³² 2777 R⁸⁶ G²⁹ 2778 R⁸⁶ G³⁰ 2779 R⁸⁶ G³¹ 2780 R⁸⁶ G³² 2781 R⁸⁷ G²⁹ 2782 R⁸⁷ G³⁰ 2783 R⁸⁷ G³¹ 2784 R⁸⁷ G³² 2785 R¹ G³³ 2786 R¹ G³⁴ 2787 R¹ G³⁵ 2788 R¹ G³⁶ 2789 R² G³³ 2790 R² G³⁴ 2791 R² G³⁵ 2792 R² G³⁶ 2793 R³ G³³ 2794 R³ G³⁴ 2795 R³ G³⁵ 2796 R³ G³⁶ 2797 R⁴ G³³ 2798 R⁴ G³⁴ 2799 R⁴ G³⁵ 2800 R⁴ G³⁶ 2801 R⁵ G³³ 2802 R⁵ G³⁴ 2803 R⁵ G³⁵ 2804 R⁵ G³⁶ 2805 R⁶ G³³ 2806 R⁶ G³⁴ 2807 R⁶ G³⁵ 2808 R⁶ G³⁶ 2809 R⁷ G³³ 2810 R⁷ G³⁴ 2811 R⁷ G³⁵ 2812 R⁷ G³⁶ 2813 R⁸ G³³ 2814 R⁸ G³⁴ 2815 R⁸ G³⁵ 2816 R⁸ G³⁶ 2817 R⁹ G³³ 2818 R⁹ G³⁴ 2819 R⁹ G³⁵ 2820 R⁹ G³⁶ 2821 R¹⁰ G³³ 2822 R¹⁰ G³⁴ 2823 R¹⁰ G³⁵ 2824 R¹⁰ G³⁶ 2825 R¹¹ G³³ 2826 R¹¹ G³⁴ 2827 R¹¹ G³⁵ 2828 R¹¹ G³⁶ 2829 R¹² G³³ 2830 R¹² G³⁴ 2831 R¹² G³⁵ 2832 R¹² G³⁶ 2833 R¹³ G³³ 2834 R¹³ G³⁴ 2835 R¹³ G³⁵ 2836 R¹³ G³⁶ 2837 R¹⁴ G³³ 2838 R¹⁴ G³⁴ 2839 R¹⁴ G³⁵ 2840 R¹⁴ G³⁶ 2841 R¹⁵ G³³ 2842 R¹⁵ G³⁴ 2843 R¹⁵ G³⁵ 2844 R¹⁵ G³⁶ 2845 R¹⁶ G³³ 2846 R¹⁶ G³⁴ 2847 R¹⁶ G³⁵ 2848 R¹⁶ G³⁶ 2849 R¹⁷ G³³ 2850 R¹⁷ G³⁴ 2851 R¹⁷ G³⁵ 2852 R¹⁷ G³⁶ 2853 R¹⁸ G³³ 2854 R¹⁸ G³⁴ 2855 R¹⁸ G³⁵ 2856 R¹⁸ G³⁶ 2857 R¹⁹ G³³ 2858 R¹⁹ G³⁴ 2859 R¹⁹ G³⁵ 2860 R¹⁹ G³⁶ 2861 R²⁰ G³³ 2862 R²⁰ G³⁴ 2863 R²⁰ G³⁵ 2864 R²⁰ G³⁶ 2865 R²¹ G³³ 2866 R²¹ G³⁴ 2867 R²¹ G³⁵ 2868 R²¹ G³⁶ 2869 R²² G³³ 2870 R²² G³⁴ 2871 R²² G³⁵ 2872 R²² G³⁶ 2873 R²³ G³³ 2874 R²³ G³⁴ 2875 R²³ G³⁵ 2876 R²³ G³⁶ 2877 R²⁴ G³³ 2878 R²⁴ G³⁴ 2879 R²⁴ G³⁵ 2880 R²⁴ G³⁶ 2881 R²⁵ G³³ 2882 R²⁵ G³⁴ 2883 R²⁵ G³⁵ 2884 R²⁵ G³⁶ 2885 R²⁶ G³³ 2886 R²⁶ G³⁴ 2887 R²⁶ G³⁵ 2888 R²⁶ G³⁶ 2889 R²⁷ G³³ 2890 R²⁷ G³⁴ 2891 R²⁷ G³⁵ 2892 R²⁷ G³⁶ 2893 R²⁸ G³³ 2894 R²⁸ G³⁴ 2895 R²⁸ G³⁵ 2896 R²⁸ G³⁶ 2897 R²⁹ G³³ 2898 R²⁹ G³⁴ 2899 R²⁹ G³⁵ 2900 R²⁹ G³⁶ 2901 R³⁰ G³³ 2902 R³⁰ G³⁴ 2903 R³⁰ G³⁵ 2904 R³⁰ G³⁶ 2905 R³¹ G³³ 2906 R³¹ G³⁴ 2907 R³¹ G³⁵ 2908 R³¹ G³⁶ 2909 R³² G³³ 2910 R³² G³⁴ 2911 R³² G³⁵ 2912 R³² G³⁶ 2913 R³³ G³³ 2914 R³³ G³⁴ 2915 R³³ G³⁵ 2916 R³³ G³⁶ 2917 R³⁴ G³³ 2918 R³⁴ G³⁴ 2919 R³⁴ G³⁵ 2920 R³⁴ G³⁶ 2921 R³⁵ G³³ 2922 R³⁵ G³⁴ 2923 R³⁵ G³⁵ 2924 R³⁵ G³⁶ 2925 R³⁶ G³³ 2926 R³⁶ G³⁴ 2927 R³⁶ G³⁵ 2928 R³⁶ G³⁶ 2929 R³⁷ G³³ 2930 R³⁷ G³⁴ 2931 R³⁷ G³⁵ 2932 R³⁷ G³⁶ 2933 R³⁸ G³³ 2934 R³⁸ G³⁴ 2935 R³⁸ G³⁵ 2936 R³⁸ G³⁶ 2937 R³⁹ G³³ 2938 R³⁹ G³⁴ 2939 R³⁹ G³⁵ 2940 R³⁹ G³⁶ 2941 R⁴⁰ G³³ 2942 R⁴⁰ G³⁴ 2943 R⁴⁰ G³⁵ 2944 R⁴⁰ G³⁶ 2945 R⁴¹ G³³ 2946 R⁴¹ G³⁴ 2947 R⁴¹ G³⁵ 2948 R⁴¹ G³⁶ 2949 R⁴² G³³ 2950 R⁴² G³⁴ 2951 R⁴² G³⁵ 2952 R⁴² G³⁶ 2953 R⁴³ G³³ 2954 R⁴³ G³⁴ 2955 R⁴³ G³⁵ 2956 R⁴³ G³⁶ 2957 R⁴⁴ G³³ 2958 R⁴⁴ G³⁴ 2959 R⁴⁴ G³⁵ 2960 R⁴⁴ G³⁶ 2961 R⁴⁵ G³³ 2962 R⁴⁵ G³⁴ 2963 R⁴⁵ G³⁵ 2964 R⁴⁵ G³⁶ 2965 R⁴⁶ G³³ 2966 R⁴⁶ G³⁴ 2967 R⁴⁶ G³⁵ 2968 R⁴⁶ G³⁶ 2969 R⁴⁷ G³³ 2970 R⁴⁷ G³⁴ 2971 R⁴⁷ G³⁵ 2972 R⁴⁷ G³⁶ 2973 R⁴⁸ G³³ 2974 R⁴⁸ G³⁴ 2975 R⁴⁸ G³⁵ 2976 R⁴⁸ G³⁶ 2977 R⁴⁹ G³³ 2978 R⁴⁹ G³⁴ 2979 R⁴⁹ G³⁵ 2980 R⁴⁹ G³⁶ 2981 R⁵⁰ G³³ 2982 R⁵⁰ G³⁴ 2983 R⁵⁰ G³⁵ 2984 R⁵⁰ G³⁶ 2985 R⁵¹ G³³ 2986 R⁵¹ G³⁴ 2987 R⁵¹ G³⁵ 2988 R⁵¹ G³⁶ 2989 R⁵² G³³ 2990 R⁵² G³⁴ 2991 R⁵² G³⁵ 2992 R⁵² G³⁶ 2993 R⁵³ G³³ 2994 R⁵³ G³⁴ 2995 R⁵³ G³⁵ 2996 R⁵³ G³⁶ 2997 R⁵⁴ G³³ 2998 R⁵⁴ G³⁴ 2999 R⁵⁴ G³⁵ 3000 R⁵⁴ G³⁶ 3001 R⁵⁵ G³³ 3002 R⁵⁵ G³⁴ 3003 R⁵⁵ G³⁵ 3004 R⁵⁵ G³⁶ 3005 R⁵⁶ G³³ 3006 R⁵⁶ G³⁴ 3007 R⁵⁶ G³⁵ 3008 R⁵⁶ G³⁶ 3009 R⁵⁷ G³³ 3010 R⁵⁷ G³⁴ 3011 R⁵⁷ G³⁵ 3012 R⁵⁷ G³⁶ 3013 R⁵⁸ G³³ 3014 R⁵⁸ G³⁴ 3015 R⁵⁸ G³⁵ 3016 R⁵⁸ G³⁶ 3017 R⁵⁹ G³³ 3018 R⁵⁹ G³⁴ 3019 R⁵⁹ G³⁵ 3020 R⁵⁹ G³⁶ 3021 R⁶⁰ G³³ 3022 R⁶⁰ G³⁴ 3023 R⁶⁰ G³⁵ 3024 R⁶⁰ G³⁶ 3025 R⁶¹ G³³ 3026 R⁶¹ G³⁴ 3027 R⁶¹ G³⁵ 3028 R⁶¹ G³⁶ 3029 R⁶² G³³ 3030 R⁶² G³⁴ 3031 R⁶² G³⁵ 3032 R⁶² G³⁶ 3033 R⁶³ G³³ 3034 R⁶³ G³⁴ 3035 R⁶³ G³⁵ 3036 R⁶³ G³⁶ 3037 R⁶⁴ G³³ 3038 R⁶⁴ G³⁴ 3039 R⁶⁴ G³⁵ 3040 R⁶⁴ G³⁶ 3041 R⁶⁵ G³³ 3042 R⁶⁵ G³⁴ 3043 R⁶⁵ G³⁵ 3044 R⁶⁵ G³⁶ 3045 R⁶⁶ G³³ 3046 R⁶⁶ G³⁴ 3047 R⁶⁶ G³⁵ 3048 R⁶⁶ G³⁶ 3049 R⁶⁷ G³³ 3050 R⁶⁷ G³⁴ 3051 R⁶⁷ G³⁵ 3052 R⁶⁷ G³⁶ 3053 R⁶⁸ G³³ 3054 R⁶⁸ G³⁴ 3055 R⁶⁸ G³⁵ 3056 R⁶⁸ G³⁶ 3057 R⁶⁹ G³³ 3058 R⁶⁹ G³⁴ 3059 R⁶⁹ G³⁵ 3060 R⁶⁹ G³⁶ 3061 R⁷⁰ G³³ 3062 R⁷⁰ G³⁴ 3063 R⁷⁰ G³⁵ 3064 R⁷⁰ G³⁶ 3065 R⁷¹ G³³ 3066 R⁷¹ G³⁴ 3067 R⁷¹ G³⁵ 3068 R⁷¹ G³⁶ 3069 R⁷² G³³ 3070 R⁷² G³⁴ 3071 R⁷² G³⁵ 3072 R⁷² G³⁶ 3073 R⁷³ G³³ 3074 R⁷³ G³⁴ 3075 R⁷³ G³⁵ 3076 R⁷³ G³⁶ 3077 R⁷⁴ G³³ 3078 R⁷⁴ G³⁴ 3079 R⁷⁴ G³⁵ 3080 R⁷⁴ G³⁶ 3081 R⁷⁵ G³³ 3082 R⁷⁵ G³⁴ 3083 R⁷⁵ G³⁵ 3084 R⁷⁵ G³⁶ 3085 R⁷⁶ G³³ 3086 R⁷⁶ G³⁴ 3087 R⁷⁶ G³⁵ 3088 R⁷⁶ G³⁶ 3089 R⁷⁷ G³³ 3090 R⁷⁷ G³⁴ 3091 R⁷⁷ G³⁵ 3092 R⁷⁷ G³⁶ 3093 R⁷⁸ G³³ 3094 R⁷⁸ G³⁴ 3095 R⁷⁸ G³⁵ 3096 R⁷⁸ G³⁶ 3097 R⁷⁹ G³³ 3098 R⁷⁹ G³⁴ 3099 R⁷⁹ G³⁵ 3100 R⁷⁹ G³⁶ 3101 R⁸⁰ G³³ 3102 R⁸⁰ G³⁴ 3103 R⁸⁰ G³⁵ 3104 R⁸⁰ G³⁶ 3105 R⁸¹ G³³ 3106 R⁸¹ G³⁴ 3107 R⁸¹ G³⁵ 3108 R⁸¹ G³⁶ 3109 R⁸² G³³ 3110 R⁸² G³⁴ 3111 R⁸² G³⁵ 3112 R⁸² G³⁶ 3113 R⁸³ G³³ 3114 R⁸³ G³⁴ 3115 R⁸³ G³⁵ 3116 R⁸³ G³⁶ 3117 R⁸⁴ G³³ 3118 R⁸⁴ G³⁴ 3119 R⁸⁴ G³⁵ 3120 R⁸⁴ G³⁶ 3121 R⁸⁵ G³³ 3122 R⁸⁵ G³⁴ 3123 R⁸⁵ G³⁵ 3124 R⁸⁵ G³⁶ 3125 R⁸⁶ G³³ 3126 R⁸⁶ G³⁴ 3127 R⁸⁶ G³⁵ 3128 R⁸⁶ G³⁶ 3129 R⁸⁷ G³³ 3130 R⁸⁷ G³⁴ 3131 R⁸⁷ G³⁵ 3132 R⁸⁷ G³⁶ 3133 R¹ G³⁷ 3134 R¹ G³⁸ 3135 R¹ G³⁹ 3136 R¹ G⁴⁰ 3137 R² G³⁷ 3138 R² G³⁸ 3139 R² G³⁹ 3140 R² G⁴⁰ 3141 R³ G³⁷ 3142 R³ G³⁸ 3143 R³ G³⁹ 3144 R³ G⁴⁰ 3145 R⁴ G³⁷ 3146 R⁴ G³⁸ 3147 R⁴ G³⁹ 3148 R⁴ G⁴⁰ 3149 R⁵ G³⁷ 3150 R⁵ G³⁸ 3151 R⁵ G³⁹ 3152 R⁵ G⁴⁰ 3153 R⁶ G³⁷ 3154 R⁶ G³⁸ 3155 R⁶ G³⁹ 3156 R⁶ G⁴⁰ 3157 R⁷ G³⁷ 3158 R⁷ G³⁸ 3159 R⁷ G³⁹ 3160 R⁷ G⁴⁰ 3161 R⁸ G³⁷ 3162 R⁸ G³⁸ 3163 R⁸ G³⁹ 3164 R⁸ G⁴⁰ 3165 R⁹ G³⁷ 3166 R⁹ G³⁸ 3167 R⁹ G³⁹ 3168 R⁹ G⁴⁰ 3169 R¹⁰ G³⁷ 3170 R¹⁰ G³⁸ 3171 R¹⁰ G³⁹ 3172 R¹⁰ G⁴⁰ 3173 R¹¹ G³⁷ 3174 R¹¹ G³⁸ 3175 R¹¹ G³⁹ 3176 R¹¹ G⁴⁰ 3177 R¹² G³⁷ 3178 R¹² G³⁸ 3179 R¹² G³⁹ 3180 R¹² G⁴⁰ 3181 R¹³ G³⁷ 3182 R¹³ G³⁸ 3183 R¹³ G³⁹ 3184 R¹³ G⁴⁰ 3185 R¹⁴ G³⁷ 3186 R¹⁴ G³⁸ 3187 R¹⁴ G³⁹ 3188 R¹⁴ G⁴⁰ 3189 R¹⁵ G³⁷ 3190 R¹⁵ G³⁸ 3191 R¹⁵ G³⁹ 3192 R¹⁵ G⁴⁰ 3193 R¹⁶ G³⁷ 3194 R¹⁶ G³⁸ 3195 R¹⁶ G³⁹ 3196 R¹⁶ G⁴⁰ 3197 R¹⁷ G³⁷ 3198 R¹⁷ G³⁸ 3199 R¹⁷ G³⁹ 3200 R¹⁷ G⁴⁰ 3201 R¹⁸ G³⁷ 3202 R¹⁸ G³⁸ 3203 R¹⁸ G³⁹ 3204 R¹⁸ G⁴⁰ 3205 R¹⁹ G³⁷ 3206 R¹⁹ G³⁸ 3207 R¹⁹ G³⁹ 3208 R¹⁹ G⁴⁰ 3209 R²⁰ G³⁷ 3210 R²⁰ G³⁸ 3211 R²⁰ G³⁹ 3212 R²⁰ G⁴⁰ 3213 R²¹ G³⁷ 3214 R²¹ G³⁸ 3215 R²¹ G³⁹ 3216 R²¹ G⁴⁰ 3217 R²² G³⁷ 3218 R²² G³⁸ 3219 R²² G³⁹ 3220 R²² G⁴⁰ 3221 R²³ G³⁷ 3222 R²³ G³⁸ 3223 R²³ G³⁹ 3224 R²³ G⁴⁰ 3225 R²⁴ G³⁷ 3226 R²⁴ G³⁸ 3227 R²⁴ G³⁹ 3228 R²⁴ G⁴⁰ 3229 R²⁵ G³⁷ 3230 R²⁵ G³⁸ 3231 R²⁵ G³⁹ 3232 R²⁵ G⁴⁰ 3233 R²⁶ G³⁷ 3234 R²⁶ G³⁸ 3235 R²⁶ G³⁹ 3236 R²⁶ G⁴⁰ 3237 R²⁷ G³⁷ 3238 R²⁷ G³⁸ 3239 R²⁷ G³⁹ 3240 R²⁷ G⁴⁰ 3241 R²⁸ G³⁷ 3242 R²⁸ G³⁸ 3243 R²⁸ G³⁹ 3244 R²⁸ G⁴⁰ 3245 R²⁹ G³⁷ 3246 R²⁹ G³⁸ 3247 R²⁹ G³⁹ 3248 R²⁹ G⁴⁰ 3249 R³⁰ G³⁷ 3250 R³⁰ G³⁸ 3251 R³⁰ G³⁹ 3252 R³⁰ G⁴⁰ 3253 R³¹ G³⁷ 3254 R³¹ G³⁸ 3255 R³¹ G³⁹ 3256 R³¹ G⁴⁰ 3257 R³² G³⁷ 3258 R³² G³⁸ 3259 R³² G³⁹ 3260 R³² G⁴⁰ 3261 R³³ G³⁷ 3262 R³³ G³⁸ 3263 R³³ G³⁹ 3264 R³³ G⁴⁰ 3265 R³⁴ G³⁷ 3266 R³⁴ G³⁸ 3267 R³⁴ G³⁹ 3268 R³⁴ G⁴⁰ 3269 R³⁵ G³⁷ 3270 R³⁵ G³⁸ 3271 R³⁵ G³⁹ 3272 R³⁵ G⁴⁰ 3273 R³⁶ G³⁷ 3274 R³⁶ G³⁸ 3275 R³⁶ G³⁹ 3276 R³⁶ G⁴⁰ 3277 R³⁷ G³⁷ 3278 R³⁷ G³⁸ 3279 R³⁷ G³⁹ 3280 R³⁷ G⁴⁰ 3281 R³⁸ G³⁷ 3282 R³⁸ G³⁸ 3283 R³⁸ G³⁹ 3284 R³⁸ G⁴⁰ 3285 R³⁹ G³⁷ 3286 R³⁹ G³⁸ 3287 R³⁹ G³⁹ 3288 R³⁹ G⁴⁰ 3289 R⁴⁰ G³⁷ 3290 R⁴⁰ G³⁸ 3291 R⁴⁰ G³⁹ 3292 R⁴⁰ G⁴⁰ 3293 R⁴¹ G³⁷ 3294 R⁴¹ G³⁸ 3295 R⁴¹ G³⁹ 3296 R⁴¹ G⁴⁰ 3297 R⁴² G³⁷ 3298 R⁴² G³⁸ 3299 R⁴² G³⁹ 3300 R⁴² G⁴⁰ 3301 R⁴³ G³⁷ 3302 R⁴³ G³⁸ 3303 R⁴³ G³⁹ 3304 R⁴³ G⁴⁰ 3305 R⁴⁴ G³⁷ 3306 R⁴⁴ G³⁸ 3307 R⁴⁴ G³⁹ 3308 R⁴⁴ G⁴⁰ 3309 R⁴⁵ G³⁷ 3310 R⁴⁵ G³⁸ 3311 R⁴⁵ G³⁹ 3312 R⁴⁵ G⁴⁰ 3313 R⁴⁶ G³⁷ 3314 R⁴⁶ G³⁸ 3315 R⁴⁶ G³⁹ 3316 R⁴⁶ G⁴⁰ 3317 R⁴⁷ G³⁷ 3318 R⁴⁷ G³⁸ 3319 R⁴⁷ G³⁹ 3320 R⁴⁷ G⁴⁰ 3321 R⁴⁸ G³⁷ 3322 R⁴⁸ G³⁸ 3323 R⁴⁸ G³⁹ 3324 R⁴⁸ G⁴⁰ 3325 R⁴⁹ G³⁷ 3326 R⁴⁹ G³⁸ 3327 R⁴⁹ G³⁹ 3328 R⁴⁹ G⁴⁰ 3329 R⁵⁰ G³⁷ 3330 R⁵⁰ G³⁸ 3331 R⁵⁰ G³⁹ 3332 R⁵⁰ G⁴⁰ 3333 R⁵¹ G³⁷ 3334 R⁵¹ G³⁸ 3335 R⁵¹ G³⁹ 3336 R⁵¹ G⁴⁰ 3337 R⁵² G³⁷ 3338 R⁵² G³⁸ 3339 R⁵² G³⁹ 3340 R⁵² G⁴⁰ 3341 R⁵³ G³⁷ 3342 R⁵³ G³⁸ 3343 R⁵³ G³⁹ 3344 R⁵³ G⁴⁰ 3345 R⁵⁴ G³⁷ 3346 R⁵⁴ G³⁸ 3347 R⁵⁴ G³⁹ 3348 R⁵⁴ G⁴⁰ 3349 R⁵⁵ G³⁷ 3350 R⁵⁵ G³⁸ 3351 R⁵⁵ G³⁹ 3352 R⁵⁵ G⁴⁰ 3353 R⁵⁶ G³⁷ 3354 R⁵⁶ G³⁸ 3355 R⁵⁶ G³⁹ 3356 R⁵⁶ G⁴⁰ 3357 R⁵⁷ G³⁷ 3358 R⁵⁷ G³⁸ 3359 R⁵⁷ G³⁹ 3360 R⁵⁷ G⁴⁰ 3361 R⁵⁸ G³⁷ 3362 R⁵⁸ G³⁸ 3363 R⁵⁸ G³⁹ 3364 R⁵⁸ G⁴⁰ 3365 R⁵⁹ G³⁷ 3366 R⁵⁹ G³⁸ 3367 R⁵⁹ G³⁹ 3368 R⁵⁹ G⁴⁰ 3369 R⁶⁰ G³⁷ 3370 R⁶⁰ G³⁸ 3371 R⁶⁰ G³⁹ 3372 R⁶⁰ G⁴⁰ 3373 R⁶¹ G³⁷ 3374 R⁶¹ G³⁸ 3375 R⁶¹ G³⁹ 3376 R⁶¹ G⁴⁰ 3377 R⁶² G³⁷ 3378 R⁶² G³⁸ 3379 R⁶² G³⁹ 3380 R⁶² G⁴⁰ 3381 R⁶³ G³⁷ 3382 R⁶³ G³⁸ 3383 R⁶³ G³⁹ 3384 R⁶³ G⁴⁰ 3385 R⁶⁴ G³⁷ 3386 R⁶⁴ G³⁸ 3387 R⁶⁴ G³⁹ 3388 R⁶⁴ G⁴⁰ 3389 R⁶⁵ G³⁷ 3390 R⁶⁵ G³⁸ 3391 R⁶⁵ G³⁹ 3392 R⁶⁵ G⁴⁰ 3393 R⁶⁶ G³⁷ 3394 R⁶⁶ G³⁸ 3395 R⁶⁶ G³⁹ 3396 R⁶⁶ G⁴⁰ 3397 R⁶⁷ G³⁷ 3398 R⁶⁷ G³⁸ 3399 R⁶⁷ G³⁹ 3400 R⁶⁷ G⁴⁰ 3401 R⁶⁸ G³⁷ 3402 R⁶⁸ G³⁸ 3403 R⁶⁸ G³⁹ 3404 R⁶⁸ G⁴⁰ 3405 R⁶⁹ G³⁷ 3406 R⁶⁹ G³⁸ 3407 R⁶⁹ G³⁹ 3408 R⁶⁹ G⁴⁰ 3409 R⁷⁰ G³⁷ 3410 R⁷⁰ G³⁸ 3411 R⁷⁰ G³⁹ 3412 R⁷⁰ G⁴⁰ 3413 R⁷¹ G³⁷ 3414 R⁷¹ G³⁸ 3415 R⁷¹ G³⁹ 3416 R⁷¹ G⁴⁰ 3417 R⁷² G³⁷ 3418 R⁷² G³⁸ 3419 R⁷² G³⁹ 3420 R⁷² G⁴⁰ 3421 R⁷³ G³⁷ 3422 R⁷³ G³⁸ 3423 R⁷³ G³⁹ 3424 R⁷³ G⁴⁰ 3425 R⁷⁴ G³⁷ 3426 R⁷⁴ G³⁸ 3427 R⁷⁴ G³⁹ 3428 R⁷⁴ G⁴⁰ 3429 R⁷⁵ G³⁷ 3430 R⁷⁵ G³⁸ 3431 R⁷⁵ G³⁹ 3432 R⁷⁵ G⁴⁰ 3433 R⁷⁶ G³⁷ 3434 R⁷⁶ G³⁸ 3435 R⁷⁶ G³⁹ 3436 R⁷⁶ G⁴⁰ 3437 R⁷⁷ G³⁷ 3438 R⁷⁷ G³⁸ 3439 R⁷⁷ G³⁹ 3440 R⁷⁷ G⁴⁰ 3441 R⁷⁸ G³⁷ 3442 R⁷⁸ G³⁸ 3443 R⁷⁸ G³⁹ 3444 R⁷⁸ G⁴⁰ 3445 R⁷⁹ G³⁷ 3446 R⁷⁹ G³⁸ 3447 R⁷⁹ G³⁹ 3448 R⁷⁹ G⁴⁰ 3449 R⁸⁰ G³⁷ 3450 R⁸⁰ G³⁸ 3451 R⁸⁰ G³⁹ 3452 R⁸⁰ G⁴⁰ 3453 R⁸¹ G³⁷ 3454 R⁸¹ G³⁸ 3455 R⁸¹ G³⁹ 3456 R⁸¹ G⁴⁰ 3457 R⁸² G³⁷ 3458 R⁸² G³⁸ 3459 R⁸² G³⁹ 3460 R⁸² G⁴⁰ 3461 R⁸³ G³⁷ 3462 R⁸³ G³⁸ 3463 R⁸³ G³⁹ 3464 R⁸³ G⁴⁰ 3465 R⁸⁴ G³⁷ 3466 R⁸⁴ G³⁸ 3467 R⁸⁴ G³⁹ 3468 R⁸⁴ G⁴⁰ 3469 R⁸⁵ G³⁷ 3470 R⁸⁵ G³⁸ 3471 R⁸⁵ G³⁹ 3472 R⁸⁵ G⁴⁰ 3473 R⁸⁶ G³⁷ 3474 R⁸⁶ G³⁸ 3475 R⁸⁶ G³⁹ 3476 R⁸⁶ G⁴⁰ 3477 R⁸⁷ G³⁷ 3478 R⁸⁷ G³⁸ 3479 R⁸⁷ G³⁹ 3480 R⁸⁷ G⁴⁰ 3481 R¹ G⁴¹ 3482 R¹ G⁴² 3483 R¹ G⁴³ 3484 R¹ G⁴⁴ 3485 R² G⁴¹ 3486 R² G⁴² 3487 R² G⁴³ 3488 R² G⁴⁴ 3489 R³ G⁴¹ 3490 R³ G⁴² 3491 R³ G⁴³ 3492 R³ G⁴⁴ 3493 R⁴ G⁴¹ 3494 R⁴ G⁴² 3495 R⁴ G⁴³ 3496 R⁴ G⁴⁴ 3497 R⁵ G⁴¹ 3498 R⁵ G⁴² 3499 R⁵ G⁴³ 3500 R⁵ G⁴⁴ 3501 R⁶ G⁴¹ 3502 R⁶ G⁴² 3503 R⁶ G⁴³ 3504 R⁶ G⁴⁴ 3505 R⁷ G⁴¹ 3506 R⁷ G⁴² 3507 R⁷ G⁴³ 3508 R⁷ G⁴⁴ 3509 R⁸ G⁴¹ 3510 R⁸ G⁴² 3511 R⁸ G⁴³ 3512 R⁸ G⁴⁴ 3513 R⁹ G⁴¹ 3514 R⁹ G⁴² 3515 R⁹ G⁴³ 3516 R⁹ G⁴⁴ 3517 R¹⁰ G⁴¹ 3518 R¹⁰ G⁴² 3519 R¹⁰ G⁴³ 3520 R¹⁰ G⁴⁴ 3521 R¹¹ G⁴¹ 3522 R¹¹ G⁴² 3523 R¹¹ G⁴³ 3524 R¹¹ G⁴⁴ 3525 R¹² G⁴¹ 3526 R¹² G⁴² 3527 R¹² G⁴³ 3528 R¹² G⁴⁴ 3529 R¹³ G⁴¹ 3530 R¹³ G⁴² 3531 R¹³ G⁴³ 3532 R¹³ G⁴⁴ 3533 R¹⁴ G⁴¹ 3534 R¹⁴ G⁴² 3535 R¹⁴ G⁴³ 3536 R¹⁴ G⁴⁴ 3537 R¹⁵ G⁴¹ 3538 R¹⁵ G⁴² 3539 R¹⁵ G⁴³ 3540 R¹⁵ G⁴⁴ 3541 R¹⁶ G⁴¹ 3542 R¹⁶ G⁴² 3543 R¹⁶ G⁴³ 3544 R¹⁶ G⁴⁴ 3545 R¹⁷ G⁴¹ 3546 R¹⁷ G⁴² 3547 R¹⁷ G⁴³ 3548 R¹⁷ G⁴⁴ 3549 R¹⁸ G⁴¹ 3550 R¹⁸ G⁴² 3551 R¹⁸ G⁴³ 3552 R¹⁸ G⁴⁴ 3553 R¹⁹ G⁴¹ 3554 R¹⁹ G⁴² 3555 R¹⁹ G⁴³ 3556 R¹⁹ G⁴⁴ 3557 R²⁰ G⁴¹ 3558 R²⁰ G⁴² 3559 R²⁰ G⁴³ 3560 R²⁰ G⁴⁴ 3561 R²¹ G⁴¹ 3562 R²¹ G⁴² 3563 R²¹ G⁴³ 3564 R²¹ G⁴⁴ 3565 R²² G⁴¹ 3566 R²² G⁴² 3567 R²² G⁴³ 3568 R²² G⁴⁴ 3569 R²³ G⁴¹ 3570 R²³ G⁴² 3571 R²³ G⁴³ 3572 R²³ G⁴⁴ 3573 R²⁴ G⁴¹ 3574 R²⁴ G⁴² 3575 R²⁴ G⁴³ 3576 R²⁴ G⁴⁴ 3577 R²⁵ G⁴¹ 3578 R²⁵ G⁴² 3579 R²⁵ G⁴³ 3580 R²⁵ G⁴⁴ 3581 R²⁶ G⁴¹ 3582 R²⁶ G⁴² 3583 R²⁶ G⁴³ 3584 R²⁶ G⁴⁴ 3585 R²⁷ G⁴¹ 3586 R²⁷ G⁴² 3587 R²⁷ G⁴³ 3588 R²⁷ G⁴⁴ 3589 R²⁸ G⁴¹ 3590 R²⁸ G⁴² 3591 R²⁸ G⁴³ 3592 R²⁸ G⁴⁴ 3593 R²⁹ G⁴¹ 3594 R²⁹ G⁴² 3595 R²⁹ G⁴³ 3596 R²⁹ G⁴⁴ 3597 R³⁰ G⁴¹ 3598 R³⁰ G⁴² 3599 R³⁰ G⁴³ 3600 R³⁰ G⁴⁴ 3601 R³¹ G⁴¹ 3602 R³¹ G⁴² 3603 R³¹ G⁴³ 3604 R³¹ G⁴⁴ 3605 R³² G⁴¹ 3606 R³² G⁴² 3607 R³² G⁴³ 3608 R³² G⁴⁴ 3609 R³³ G⁴¹ 3610 R³³ G⁴² 3611 R³³ G⁴³ 3612 R³³ G⁴⁴ 3613 R³⁴ G⁴¹ 3614 R³⁴ G⁴² 3615 R³⁴ G⁴³ 3616 R³⁴ G⁴⁴ 3617 R³⁵ G⁴¹ 3618 R³⁵ G⁴² 3619 R³⁵ G⁴³ 3620 R³⁵ G⁴⁴ 3621 R³⁶ G⁴¹ 3622 R³⁶ G⁴² 3623 R³⁶ G⁴³ 3624 R³⁶ G⁴⁴ 3625 R³⁷ G⁴¹ 3626 R³⁷ G⁴² 3627 R³⁷ G⁴³ 3628 R³⁷ G⁴⁴ 3629 R³⁸ G⁴¹ 3630 R³⁸ G⁴² 3631 R³⁸ G⁴³ 3632 R³⁸ G⁴⁴ 3633 R³⁹ G⁴¹ 3634 R³⁹ G⁴² 3635 R³⁹ G⁴³ 3636 R³⁹ G⁴⁴ 3637 R⁴⁰ G⁴¹ 3638 R⁴⁰ G⁴² 3639 R⁴⁰ G⁴³ 3640 R⁴⁰ G⁴⁴ 3641 R⁴¹ G⁴¹ 3642 R⁴¹ G⁴² 3643 R⁴¹ G⁴³ 3644 R⁴¹ G⁴⁴ 3645 R⁴² G⁴¹ 3646 R⁴² G⁴² 3647 R⁴² G⁴³ 3648 R⁴² G⁴⁴ 3649 R⁴³ G⁴¹ 3650 R⁴³ G⁴² 3651 R⁴³ G⁴³ 3652 R⁴³ G⁴⁴ 3653 R⁴⁴ G⁴¹ 3654 R⁴⁴ G⁴² 3655 R⁴⁴ G⁴³ 3656 R⁴⁴ G⁴⁴ 3657 R⁴⁵ G⁴¹ 3658 R⁴⁵ G⁴² 3659 R⁴⁵ G⁴³ 3660 R⁴⁵ G⁴⁴ 3661 R⁴⁶ G⁴¹ 3662 R⁴⁶ G⁴² 3663 R⁴⁶ G⁴³ 3664 R⁴⁶ G⁴⁴ 3665 R⁴⁷ G⁴¹ 3666 R⁴⁷ G⁴² 3667 R⁴⁷ G⁴³ 3668 R⁴⁷ G⁴⁴ 3669 R⁴⁸ G⁴¹ 3670 R⁴⁸ G⁴² 3671 R⁴⁸ G⁴³ 3672 R⁴⁸ G⁴⁴ 3673 R⁴⁹ G⁴¹ 3674 R⁴⁹ G⁴² 3675 R⁴⁹ G⁴³ 3676 R⁴⁹ G⁴⁴ 3677 R⁵⁰ G⁴¹ 3678 R⁵⁰ G⁴² 3679 R⁵⁰ G⁴³ 3680 R⁵⁰ G⁴⁴ 3681 R⁵¹ G⁴¹ 3682 R⁵¹ G⁴² 3683 R⁵¹ G⁴³ 3684 R⁵¹ G⁴⁴ 3685 R⁵² G⁴¹ 3686 R⁵² G⁴² 3687 R⁵² G⁴³ 3688 R⁵² G⁴⁴ 3689 R⁵³ G⁴¹ 3690 R⁵³ G⁴² 3691 R⁵³ G⁴³ 3692 R⁵³ G⁴⁴ 3693 R⁵⁴ G⁴¹ 3694 R⁵⁴ G⁴² 3695 R⁵⁴ G⁴³ 3696 R⁵⁴ G⁴⁴ 3697 R⁵⁵ G⁴¹ 3698 R⁵⁵ G⁴² 3699 R⁵⁵ G⁴³ 3700 R⁵⁵ G⁴⁴ 3701 R⁵⁶ G⁴¹ 3702 R⁵⁶ G⁴² 3703 R⁵⁶ G⁴³ 3704 R⁵⁶ G⁴⁴ 3705 R⁵⁷ G⁴¹ 3706 R⁵⁷ G⁴² 3707 R⁵⁷ G⁴³ 3708 R⁵⁷ G⁴⁴ 3709 R⁵⁸ G⁴¹ 3710 R⁵⁸ G⁴² 3711 R⁵⁸ G⁴³ 3712 R⁵⁸ G⁴⁴ 3713 R⁵⁹ G⁴¹ 3714 R⁵⁹ G⁴² 3715 R⁵⁹ G⁴³ 3716 R⁵⁹ G⁴⁴ 3717 R⁶⁰ G⁴¹ 3718 R⁶⁰ G⁴² 3719 R⁶⁰ G⁴³ 3720 R⁶⁰ G⁴⁴ 3721 R⁶¹ G⁴¹ 3722 R⁶¹ G⁴² 3723 R⁶¹ G⁴³ 3724 R⁶¹ G⁴⁴ 3725 R⁶² G⁴¹ 3726 R⁶² G⁴² 3727 R⁶² G⁴³ 3728 R⁶² G⁴⁴ 3729 R⁶³ G⁴¹ 3730 R⁶³ G⁴² 3731 R⁶³ G⁴³ 3732 R⁶³ G⁴⁴ 3733 R⁶⁴ G⁴¹ 3734 R⁶⁴ G⁴² 3735 R⁶⁴ G⁴³ 3736 R⁶⁴ G⁴⁴ 3737 R⁶⁵ G⁴¹ 3738 R⁶⁵ G⁴² 3739 R⁶⁵ G⁴³ 3740 R⁶⁵ G⁴⁴ 3741 R⁶⁶ G⁴¹ 3742 R⁶⁶ G⁴² 3743 R⁶⁶ G⁴³ 3744 R⁶⁶ G⁴⁴ 3745 R⁶⁷ G⁴¹ 3746 R⁶⁷ G⁴² 3747 R⁶⁷ G⁴³ 3748 R⁶⁷ G⁴⁴ 3749 R⁶⁸ G⁴¹ 3750 R⁶⁸ G⁴² 3751 R⁶⁸ G⁴³ 3752 R⁶⁸ G⁴⁴ 3753 R⁶⁹ G⁴¹ 3754 R⁶⁹ G⁴² 3755 R⁶⁹ G⁴³ 3756 R⁶⁹ G⁴⁴ 3757 R⁷⁰ G⁴¹ 3758 R⁷⁰ G⁴² 3759 R⁷⁰ G⁴³ 3760 R⁷⁰ G⁴⁴ 3761 R⁷¹ G⁴¹ 3762 R⁷¹ G⁴² 3763 R⁷¹ G⁴³ 3764 R⁷¹ G⁴⁴ 3765 R⁷² G⁴¹ 3766 R⁷² G⁴² 3767 R⁷² G⁴³ 3768 R⁷² G⁴⁴ 3769 R⁷³ G⁴¹ 3770 R⁷³ G⁴² 3771 R⁷³ G⁴³ 3772 R⁷³ G⁴⁴ 3773 R⁷⁴ G⁴¹ 3774 R⁷⁴ G⁴² 3775 R⁷⁴ G⁴³ 3776 R⁷⁴ G⁴⁴ 3777 R⁷⁵ G⁴¹ 3778 R⁷⁵ G⁴² 3779 R⁷⁵ G⁴³ 3780 R⁷⁵ G⁴⁴ 3781 R⁷⁶ G⁴¹ 3782 R⁷⁶ G⁴² 3783 R⁷⁶ G⁴³ 3784 R⁷⁶ G⁴⁴ 3785 R⁷⁷ G⁴¹ 3786 R⁷⁷ G⁴² 3787 R⁷⁷ G⁴³ 3788 R⁷⁷ G⁴⁴ 3789 R⁷⁸ G⁴¹ 3790 R⁷⁸ G⁴² 3791 R⁷⁸ G⁴³ 3792 R⁷⁸ G⁴⁴ 3793 R⁷⁹ G⁴¹ 3794 R⁷⁹ G⁴² 3795 R⁷⁹ G⁴³ 3796 R⁷⁹ G⁴⁴ 3797 R⁸⁰ G⁴¹ 3798 R⁸⁰ G⁴² 3799 R⁸⁰ G⁴³ 3800 R⁸⁰ G⁴⁴ 3801 R⁸¹ G⁴¹ 3802 R⁸¹ G⁴² 3803 R⁸¹ G⁴³ 3804 R⁸¹ G⁴⁴ 3805 R⁸² G⁴¹ 3806 R⁸² G⁴² 3807 R⁸² G⁴³ 3808 R⁸² G⁴⁴ 3809 R⁸³ G⁴¹ 3810 R⁸³ G⁴² 3811 R⁸³ G⁴³ 3812 R⁸³ G⁴⁴ 3813 R⁸⁴ G⁴¹ 3814 R⁸⁴ G⁴² 3815 R⁸⁴ G⁴³ 3816 R⁸⁴ G⁴⁴ 3817 R⁸⁵ G⁴¹ 3818 R⁸⁵ G⁴² 3819 R⁸⁵ G⁴³ 3820 R⁸⁵ G⁴⁴ 3821 R⁸⁶ G⁴¹ 3822 R⁸⁶ G⁴² 3823 R⁸⁶ G⁴³ 3824 R⁸⁶ G⁴⁴ 3825 R⁸⁷ G⁴¹ 3826 R⁸⁷ G⁴² 3827 R⁸⁷ G⁴³ 3828 R⁸⁷ G⁴⁴ 3829 R¹ G⁴⁵ 3830 R¹ G⁴⁶ 3831 R¹ G⁴⁷ 3832 R¹ G⁴⁸ 3833 R² G⁴⁵ 3834 R² G⁴⁶ 3835 R² G⁴⁷ 3836 R² G⁴⁸ 3837 R³ G⁴⁵ 3838 R³ G⁴⁶ 3839 R³ G⁴⁷ 3840 R³ G⁴⁸ 3841 R⁴ G⁴⁵ 3842 R⁴ G⁴⁶ 3843 R⁴ G⁴⁷ 3844 R⁴ G⁴⁸ 3845 R⁵ G⁴⁵ 3846 R⁵ G⁴⁶ 3847 R⁵ G⁴⁷ 3848 R⁵ G⁴⁸ 3849 R⁶ G⁴⁵ 3850 R⁶ G⁴⁶ 3851 R⁶ G⁴⁷ 3852 R⁶ G⁴⁸ 3853 R⁷ G⁴⁵ 3854 R⁷ G⁴⁶ 3855 R⁷ G⁴⁷ 3856 R⁷ G⁴⁸ 3857 R⁸ G⁴⁵ 3858 R⁸ G⁴⁶ 3859 R⁸ G⁴⁷ 3860 R⁸ G⁴⁸ 3861 R⁹ G⁴⁵ 3862 R⁹ G⁴⁶ 3863 R⁹ G⁴⁷ 3864 R⁹ G⁴⁸ 3865 R¹⁰ G⁴⁵ 3866 R¹⁰ G⁴⁶ 3867 R¹⁰ G⁴⁷ 3868 R¹⁰ G⁴⁸ 3869 R¹¹ G⁴⁵ 3870 R¹¹ G⁴⁶ 3871 R¹¹ G⁴⁷ 3872 R¹¹ G⁴⁸ 3873 R¹² G⁴⁵ 3874 R¹² G⁴⁶ 3875 R¹² G⁴⁷ 3876 R¹² G⁴⁸ 3877 R¹³ G⁴⁵ 3878 R¹³ G⁴⁶ 3879 R¹³ G⁴⁷ 3880 R¹³ G⁴⁸ 3881 R¹⁴ G⁴⁵ 3882 R¹⁴ G⁴⁶ 3883 R¹⁴ G⁴⁷ 3884 R¹⁴ G⁴⁸ 3885 R¹⁵ G⁴⁵ 3886 R¹⁵ G⁴⁶ 3887 R¹⁵ G⁴⁷ 3888 R¹⁵ G⁴⁸ 3889 R¹⁶ G⁴⁵ 3890 R¹⁶ G⁴⁶ 3891 R¹⁶ G⁴⁷ 3892 R¹⁶ G⁴⁸ 3893 R¹⁷ G⁴⁵ 3894 R¹⁷ G⁴⁶ 3895 R¹⁷ G⁴⁷ 3896 R¹⁷ G⁴⁸ 3897 R¹⁸ G⁴⁵ 3898 R¹⁸ G⁴⁶ 3899 R¹⁸ G⁴⁷ 3900 R¹⁸ G⁴⁸ 3901 R¹⁹ G⁴⁵ 3902 R¹⁹ G⁴⁶ 3903 R¹⁹ G⁴⁷ 3904 R¹⁹ G⁴⁸ 3905 R²⁰ G⁴⁵ 3906 R²⁰ G⁴⁶ 3907 R²⁰ G⁴⁷ 3908 R²⁰ G⁴⁸ 3909 R²¹ G⁴⁵ 3910 R²¹ G⁴⁶ 3911 R²¹ G⁴⁷ 3912 R²¹ G⁴⁸ 3913 R²² G⁴⁵ 3914 R²² G⁴⁶ 3915 R²² G⁴⁷ 3916 R²² G⁴⁸ 3917 R²³ G⁴⁵ 3918 R²³ G⁴⁶ 3919 R²³ G⁴⁷ 3920 R²³ G⁴⁸ 3921 R²⁴ G⁴⁵ 3922 R²⁴ G⁴⁶ 3923 R²⁴ G⁴⁷ 3924 R²⁴ G⁴⁸ 3925 R²⁵ G⁴⁵ 3926 R²⁵ G⁴⁶ 3927 R²⁵ G⁴⁷ 3928 R²⁵ G⁴⁸ 3929 R²⁶ G⁴⁵ 3930 R²⁶ G⁴⁶ 3931 R²⁶ G⁴⁷ 3932 R²⁶ G⁴⁸ 3933 R²⁷ G⁴⁵ 3934 R²⁷ G⁴⁶ 3935 R²⁷ G⁴⁷ 3936 R²⁷ G⁴⁸ 3937 R²⁸ G⁴⁵ 3938 R²⁸ G⁴⁶ 3939 R²⁸ G⁴⁷ 3940 R²⁸ G⁴⁸ 3941 R²⁹ G⁴⁵ 3942 R²⁹ G⁴⁶ 3943 R²⁹ G⁴⁷ 3944 R²⁹ G⁴⁸ 3945 R³⁰ G⁴⁵ 3946 R³⁰ G⁴⁶ 3947 R³⁰ G⁴⁷ 3948 R³⁰ G⁴⁸ 3949 R³¹ G⁴⁵ 3950 R³¹ G⁴⁶ 3951 R³¹ G⁴⁷ 3952 R³¹ G⁴⁸ 3953 R³² G⁴⁵ 3954 R³² G⁴⁶ 3955 R³² G⁴⁷ 3956 R³² G⁴⁸ 3957 R³³ G⁴⁵ 3958 R³³ G⁴⁶ 3959 R³³ G⁴⁷ 3960 R³³ G⁴⁸ 3961 R³⁴ G⁴⁵ 3962 R³⁴ G⁴⁶ 3963 R³⁴ G⁴⁷ 3964 R³⁴ G⁴⁸ 3965 R³⁵ G⁴⁵ 3966 R³⁵ G⁴⁶ 3967 R³⁵ G⁴⁷ 3968 R³⁵ G⁴⁸ 3969 R³⁶ G⁴⁵ 3970 R³⁶ G⁴⁶ 3971 R³⁶ G⁴⁷ 3972 R³⁶ G⁴⁸ 3973 R³⁷ G⁴⁵ 3974 R³⁷ G⁴⁶ 3975 R³⁷ G⁴⁷ 3976 R³⁷ G⁴⁸ 3977 R³⁸ G⁴⁵ 3978 R³⁸ G⁴⁶ 3979 R³⁸ G⁴⁷ 3980 R³⁸ G⁴⁸ 3981 R³⁹ G⁴⁵ 3982 R³⁹ G⁴⁶ 3983 R³⁹ G⁴⁷ 3984 R³⁹ G⁴⁸ 3985 R⁴⁰ G⁴⁵ 3986 R⁴⁰ G⁴⁶ 3987 R⁴⁰ G⁴⁷ 3988 R⁴⁰ G⁴⁸ 3989 R⁴¹ G⁴⁵ 3990 R⁴¹ G⁴⁶ 3991 R⁴¹ G⁴⁷ 3992 R⁴¹ G⁴⁸ 3993 R⁴² G⁴⁵ 3994 R⁴² G⁴⁶ 3995 R⁴² G⁴⁷ 3996 R⁴² G⁴⁸ 3997 R⁴³ G⁴⁵ 3998 R⁴³ G⁴⁶ 3999 R⁴³ G⁴⁷ 4000 R⁴³ G⁴⁸ 4001 R⁴⁴ G⁴⁵ 4002 R⁴⁴ G⁴⁶ 4003 R⁴⁴ G⁴⁷ 4004 R⁴⁴ G⁴⁸ 4005 R⁴⁵ G⁴⁵ 4006 R⁴⁵ G⁴⁶ 4007 R⁴⁵ G⁴⁷ 4008 R⁴⁵ G⁴⁸ 4009 R⁴⁶ G⁴⁵ 4010 R⁴⁶ G⁴⁶ 4011 R⁴⁶ G⁴⁷ 4012 R⁴⁶ G⁴⁸ 4013 R⁴⁷ G⁴⁵ 4014 R⁴⁷ G⁴⁶ 4015 R⁴⁷ G⁴⁷ 4016 R⁴⁷ G⁴⁸ 4017 R⁴⁸ G⁴⁵ 4018 R⁴⁸ G⁴⁶ 4019 R⁴⁸ G⁴⁷ 4020 R⁴⁸ G⁴⁸ 4021 R⁴⁹ G⁴⁵ 4022 R⁴⁹ G⁴⁶ 4023 R⁴⁹ G⁴⁷ 4024 R⁴⁹ G⁴⁸ 4025 R⁵⁰ G⁴⁵ 4026 R⁵⁰ G⁴⁶ 4027 R⁵⁰ G⁴⁷ 4028 R⁵⁰ G⁴⁸ 4029 R⁵¹ G⁴⁵ 4030 R⁵¹ G⁴⁶ 4031 R⁵¹ G⁴⁷ 4032 R⁵¹ G⁴⁸ 4033 R⁵² G⁴⁵ 4034 R⁵² G⁴⁶ 4035 R⁵² G⁴⁷ 4036 R⁵² G⁴⁸ 4037 R⁵³ G⁴⁵ 4038 R⁵³ G⁴⁶ 4039 R⁵³ G⁴⁷ 4040 R⁵³ G⁴⁸ 4041 R⁵⁴ G⁴⁵ 4042 R⁵⁴ G⁴⁶ 4043 R⁵⁴ G⁴⁷ 4044 R⁵⁴ G⁴⁸ 4045 R⁵⁵ G⁴⁵ 4046 R⁵⁵ G⁴⁶ 4047 R⁵⁵ G⁴⁷ 4048 R⁵⁵ G⁴⁸ 4049 R⁵⁶ G⁴⁵ 4050 R⁵⁶ G⁴⁶ 4051 R⁵⁶ G⁴⁷ 4052 R⁵⁶ G⁴⁸ 4053 R⁵⁷ G⁴⁵ 4054 R⁵⁷ G⁴⁶ 4055 R⁵⁷ G⁴⁷ 4056 R⁵⁷ G⁴⁸ 4057 R⁵⁸ G⁴⁵ 4058 R⁵⁸ G⁴⁶ 4059 R⁵⁸ G⁴⁷ 4060 R⁵⁸ G⁴⁸ 4061 R⁵⁹ G⁴⁵ 4062 R⁵⁹ G⁴⁶ 4063 R⁵⁹ G⁴⁷ 4064 R⁵⁹ G⁴⁸ 4065 R⁶⁰ G⁴⁵ 4066 R⁶⁰ G⁴⁶ 4067 R⁶⁰ G⁴⁷ 4068 R⁶⁰ G⁴⁸ 4069 R⁶¹ G⁴⁵ 4070 R⁶¹ G⁴⁶ 4071 R⁶¹ G⁴⁷ 4072 R⁶¹ G⁴⁸ 4073 R⁶² G⁴⁵ 4074 R⁶² G⁴⁶ 4075 R⁶² G⁴⁷ 4076 R⁶² G⁴⁸ 4077 R⁶³ G⁴⁵ 4078 R⁶³ G⁴⁶ 4079 R⁶³ G⁴⁷ 4080 R⁶³ G⁴⁸ 4081 R⁶⁴ G⁴⁵ 4082 R⁶⁴ G⁴⁶ 4083 R⁶⁴ G⁴⁷ 4084 R⁶⁴ G⁴⁸ 4085 R⁶⁵ G⁴⁵ 4086 R⁶⁵ G⁴⁶ 4087 R⁶⁵ G⁴⁷ 4088 R⁶⁵ G⁴⁸ 4089 R⁶⁶ G⁴⁵ 4090 R⁶⁶ G⁴⁶ 4091 R⁶⁶ G⁴⁷ 4092 R⁶⁶ G⁴⁸ 4093 R⁶⁷ G⁴⁵ 4094 R⁶⁷ G⁴⁶ 4095 R⁶⁷ G⁴⁷ 4096 R⁶⁷ G⁴⁸ 4097 R⁶⁸ G⁴⁵ 4098 R⁶⁸ G⁴⁶ 4099 R⁶⁸ G⁴⁷ 4100 R⁶⁸ G⁴⁸ 4101 R⁶⁹ G⁴⁵ 4102 R⁶⁹ G⁴⁶ 4103 R⁶⁹ G⁴⁷ 4104 R⁶⁹ G⁴⁸ 4105 R⁷⁰ G⁴⁵ 4106 R⁷⁰ G⁴⁶ 4107 R⁷⁰ G⁴⁷ 4108 R⁷⁰ G⁴⁸ 4109 R⁷¹ G⁴⁵ 4110 R⁷¹ G⁴⁶ 4111 R⁷¹ G⁴⁷ 4112 R⁷¹ G⁴⁸ 4113 R⁷² G⁴⁵ 4114 R⁷² G⁴⁶ 4115 R⁷² G⁴⁷ 4116 R⁷² G⁴⁸ 4117 R⁷³ G⁴⁵ 4118 R⁷³ G⁴⁶ 4119 R⁷³ G⁴⁷ 4120 R⁷³ G⁴⁸ 4121 R⁷⁴ G⁴⁵ 4122 R⁷⁴ G⁴⁶ 4123 R⁷⁴ G⁴⁷ 4124 R⁷⁴ G⁴⁸ 4125 R⁷⁵ G⁴⁵ 4126 R⁷⁵ G⁴⁶ 4127 R⁷⁵ G⁴⁷ 4128 R⁷⁵ G⁴⁸ 4129 R⁷⁶ G⁴⁵ 4130 R⁷⁶ G⁴⁶ 4131 R⁷⁶ G⁴⁷ 4132 R⁷⁶ G⁴⁸ 4133 R⁷⁷ G⁴⁵ 4134 R⁷⁷ G⁴⁶ 4135 R⁷⁷ G⁴⁷ 4136 R⁷⁷ G⁴⁸ 4137 R⁷⁸ G⁴⁵ 4138 R⁷⁸ G⁴⁶ 4139 R⁷⁸ G⁴⁷ 4140 R⁷⁸ G⁴⁸ 4141 R⁷⁹ G⁴⁵ 4142 R⁷⁹ G⁴⁶ 4143 R⁷⁹ G⁴⁷ 4144 R⁷⁹ G⁴⁸ 4145 R⁸⁰ G⁴⁵ 4146 R⁸⁰ G⁴⁶ 4147 R⁸⁰ G⁴⁷ 4148 R⁸⁰ G⁴⁸ 4149 R⁸¹ G⁴⁵ 4150 R⁸¹ G⁴⁶ 4151 R⁸¹ G⁴⁷ 4152 R⁸¹ G⁴⁸ 4153 R⁸² G⁴⁵ 4154 R⁸² G⁴⁶ 4155 R⁸² G⁴⁷ 4156 R⁸² G⁴⁸ 4157 R⁸³ G⁴⁵ 4158 R⁸³ G⁴⁶ 4159 R⁸³ G⁴⁷ 4160 R⁸³ G⁴⁸ 4161 R⁸⁴ G⁴⁵ 4162 R⁸⁴ G⁴⁶ 4163 R⁸⁴ G⁴⁷ 4164 R⁸⁴ G⁴⁸ 4165 R⁸⁵ G⁴⁵ 4166 R⁸⁵ G⁴⁶ 4167 R⁸⁵ G⁴⁷ 4168 R⁸⁵ G⁴⁸ 4169 R⁸⁶ G⁴⁵ 4170 R⁸⁶ G⁴⁶ 4171 R⁸⁶ G⁴⁷ 4172 R⁸⁶ G⁴⁸ 4173 R⁸⁷ G⁴⁵ 4174 R⁸⁷ G⁴⁶ 4175 R⁸⁷ G⁴⁷ 4176 R⁸⁷ G⁴⁸ 4177 R¹ G⁴⁹ 4178 R¹ G⁵⁰ 4179 R¹ G⁵¹ 4180 R¹ G⁵² 4181 R² G⁴⁹ 4182 R² G⁵⁰ 4183 R² G⁵¹ 4184 R² G⁵² 4185 R³ G⁴⁹ 4186 R³ G⁵⁰ 4187 R³ G⁵¹ 4188 R³ G⁵² 4189 R⁴ G⁴⁹ 4190 R⁴ G⁵⁰ 4191 R⁴ G⁵¹ 4192 R⁴ G⁵² 4193 R⁵ G⁴⁹ 4194 R⁵ G⁵⁰ 4195 R⁵ G⁵¹ 4196 R⁵ G⁵² 4197 R⁶ G⁴⁹ 4198 R⁶ G⁵⁰ 4199 R⁶ G⁵¹ 4200 R⁶ G⁵² 4201 R⁷ G⁴⁹ 4202 R⁷ G⁵⁰ 4203 R⁷ G⁵¹ 4204 R⁷ G⁵² 4205 R⁸ G⁴⁹ 4206 R⁸ G⁵⁰ 4207 R⁸ G⁵¹ 4208 R⁸ G⁵² 4209 R⁹ G⁴⁹ 4210 R⁹ G⁵⁰ 4211 R⁹ G⁵¹ 4212 R⁹ G⁵² 4213 R¹⁰ G⁴⁹ 4214 R¹⁰ G⁵⁰ 4215 R¹⁰ G⁵¹ 4216 R¹⁰ G⁵² 4217 R¹¹ G⁴⁹ 4218 R¹¹ G⁵⁰ 4219 R¹¹ G⁵¹ 4220 R¹¹ G⁵² 4221 R¹² G⁴⁹ 4222 R¹² G⁵⁰ 4223 R¹² G⁵¹ 4224 R¹² G⁵² 4225 R¹³ G⁴⁹ 4226 R¹³ G⁵⁰ 4227 R¹³ G⁵¹ 4228 R¹³ G⁵² 4229 R¹⁴ G⁴⁹ 4230 R¹⁴ G⁵⁰ 4231 R¹⁴ G⁵¹ 4232 R¹⁴ G⁵² 4233 R¹⁵ G⁴⁹ 4234 R¹⁵ G⁵⁰ 4235 R¹⁵ G⁵¹ 4236 R¹⁵ G⁵² 4237 R¹⁶ G⁴⁹ 4238 R¹⁶ G⁵⁰ 4239 R¹⁶ G⁵¹ 4240 R¹⁶ G⁵² 4241 R¹⁷ G⁴⁹ 4242 R¹⁷ G⁵⁰ 4243 R¹⁷ G⁵¹ 4244 R¹⁷ G⁵² 4245 R¹⁸ G⁴⁹ 4246 R¹⁸ G⁵⁰ 4247 R¹⁸ G⁵¹ 4248 R¹⁸ G⁵² 4249 R¹⁹ G⁴⁹ 4250 R¹⁹ G⁵⁰ 4251 R¹⁹ G⁵¹ 4252 R¹⁹ G⁵² 4253 R²⁰ G⁴⁹ 4254 R²⁰ G⁵⁰ 4255 R²⁰ G⁵¹ 4256 R²⁰ G⁵² 4257 R²¹ G⁴⁹ 4258 R²¹ G⁵⁰ 4259 R²¹ G⁵¹ 4260 R²¹ G⁵² 4261 R²² G⁴⁹ 4262 R²² G⁵⁰ 4263 R²² G⁵¹ 4264 R²² G⁵² 4265 R²³ G⁴⁹ 4266 R²³ G⁵⁰ 4267 R²³ G⁵¹ 4268 R²³ G⁵² 4269 R²⁴ G⁴⁹ 4270 R²⁴ G⁵⁰ 4271 R²⁴ G⁵¹ 4272 R²⁴ G⁵² 4273 R²⁵ G⁴⁹ 4274 R²⁵ G⁵⁰ 4275 R²⁵ G⁵¹ 4276 R²⁵ G⁵² 4277 R²⁶ G⁴⁹ 4278 R²⁶ G⁵⁰ 4279 R²⁶ G⁵¹ 4280 R²⁶ G⁵² 4281 R²⁷ G⁴⁹ 4282 R²⁷ G⁵⁰ 4283 R²⁷ G⁵¹ 4284 R²⁷ G⁵² 4285 R²⁸ G⁴⁹ 4286 R²⁸ G⁵⁰ 4287 R²⁸ G⁵¹ 4288 R²⁸ G⁵² 4289 R²⁹ G⁴⁹ 4290 R²⁹ G⁵⁰ 4291 R²⁹ G⁵¹ 4292 R²⁹ G⁵² 4293 R³⁰ G⁴⁹ 4294 R³⁰ G⁵⁰ 4295 R³⁰ G⁵¹ 4296 R³⁰ G⁵² 4297 R³¹ G⁴⁹ 4298 R³¹ G⁵⁰ 4299 R³¹ G⁵¹ 4300 R³¹ G⁵² 4301 R³² G⁴⁹ 4302 R³² G⁵⁰ 4303 R³² G⁵¹ 4304 R³² G⁵² 4305 R³³ G⁴⁹ 4306 R³³ G⁵⁰ 4307 R³³ G⁵¹ 4308 R³³ G⁵² 4309 R³⁴ G⁴⁹ 4310 R³⁴ G⁵⁰ 4311 R³⁴ G⁵¹ 4312 R³⁴ G⁵² 4313 R³⁵ G⁴⁹ 4314 R³⁵ G⁵⁰ 4315 R³⁵ G⁵¹ 4316 R³⁵ G⁵² 4317 R³⁶ G⁴⁹ 4318 R³⁶ G⁵⁰ 4319 R³⁶ G⁵¹ 4320 R³⁶ G⁵² 4321 R³⁷ G⁴⁹ 4322 R³⁷ G⁵⁰ 4323 R³⁷ G⁵¹ 4324 R³⁷ G⁵² 4325 R³⁸ G⁴⁹ 4326 R³⁸ G⁵⁰ 4327 R³⁸ G⁵¹ 4328 R³⁸ G⁵² 4329 R³⁹ G⁴⁹ 4330 R³⁹ G⁵⁰ 4331 R³⁹ G⁵¹ 4332 R³⁹ G⁵² 4333 R⁴⁰ G⁴⁹ 4334 R⁴⁰ G⁵⁰ 4335 R⁴⁰ G⁵¹ 4336 R⁴⁰ G⁵² 4337 R⁴¹ G⁴⁹ 4338 R⁴¹ G⁵⁰ 4339 R⁴¹ G⁵¹ 4340 R⁴¹ G⁵² 4341 R⁴² G⁴⁹ 4342 R⁴² G⁵⁰ 4343 R⁴² G⁵¹ 4344 R⁴² G⁵² 4345 R⁴³ G⁴⁹ 4346 R⁴³ G⁵⁰ 4347 R⁴³ G⁵¹ 4348 R⁴³ G⁵² 4349 R⁴⁴ G⁴⁹ 4350 R⁴⁴ G⁵⁰ 4351 R⁴⁴ G⁵¹ 4352 R⁴⁴ G⁵² 4353 R⁴⁵ G⁴⁹ 4354 R⁴⁵ G⁵⁰ 4355 R⁴⁵ G⁵¹ 4356 R⁴⁵ G⁵² 4357 R⁴⁶ G⁴⁹ 4358 R⁴⁶ G⁵⁰ 4359 R⁴⁶ G⁵¹ 4360 R⁴⁶ G⁵² 4361 R⁴⁷ G⁴⁹ 4362 R⁴⁷ G⁵⁰ 4363 R⁴⁷ G⁵¹ 4364 R⁴⁷ G⁵² 4365 R⁴⁸ G⁴⁹ 4366 R⁴⁸ G⁵⁰ 4367 R⁴⁸ G⁵¹ 4368 R⁴⁸ G⁵² 4369 R⁴⁹ G⁴⁹ 4370 R⁴⁹ G⁵⁰ 4371 R⁴⁹ G⁵¹ 4372 R⁴⁹ G⁵² 4373 R⁵⁰ G⁴⁹ 4374 R⁵⁰ G⁵⁰ 4375 R⁵⁰ G⁵¹ 4376 R⁵⁰ G⁵² 4377 R⁵¹ G⁴⁹ 4378 R⁵¹ G⁵⁰ 4379 R⁵¹ G⁵¹ 4380 R⁵¹ G⁵² 4381 R⁵² G⁴⁹ 4382 R⁵² G⁵⁰ 4383 R⁵² G⁵¹ 4384 R⁵² G⁵² 4385 R⁵³ G⁴⁹ 4386 R⁵³ G⁵⁰ 4387 R⁵³ G⁵¹ 4388 R⁵³ G⁵² 4389 R⁵⁴ G⁴⁹ 4390 R⁵⁴ G⁵⁰ 4391 R⁵⁴ G⁵¹ 4392 R⁵⁴ G⁵² 4393 R⁵⁵ G⁴⁹ 4394 R⁵⁵ G⁵⁰ 4395 R⁵⁵ G⁵¹ 4396 R⁵⁵ G⁵² 4397 R⁵⁶ G⁴⁹ 4398 R⁵⁶ G⁵⁰ 4399 R⁵⁶ G⁵¹ 4400 R⁵⁶ G⁵² 4401 R⁵⁷ G⁴⁹ 4402 R⁵⁷ G⁵⁰ 4403 R⁵⁷ G⁵¹ 4404 R⁵⁷ G⁵² 4405 R⁵⁸ G⁴⁹ 4406 R⁵⁸ G⁵⁰ 4407 R⁵⁸ G⁵¹ 4408 R⁵⁸ G⁵² 4409 R⁵⁹ G⁴⁹ 4410 R⁵⁹ G⁵⁰ 4411 R⁵⁹ G⁵¹ 4412 R⁵⁹ G⁵² 4413 R⁶⁰ G⁴⁹ 4414 R⁶⁰ G⁵⁰ 4415 R⁶⁰ G⁵¹ 4416 R⁶⁰ G⁵² 4417 R⁶¹ G⁴⁹ 4418 R⁶¹ G⁵⁰ 4419 R⁶¹ G⁵¹ 4420 R⁶¹ G⁵² 4421 R⁶² G⁴⁹ 4422 R⁶² G⁵⁰ 4423 R⁶² G⁵¹ 4424 R⁶² G⁵² 4425 R⁶³ G⁴⁹ 4426 R⁶³ G⁵⁰ 4427 R⁶³ G⁵¹ 4428 R⁶³ G⁵² 4429 R⁶⁴ G⁴⁹ 4430 R⁶⁴ G⁵⁰ 4431 R⁶⁴ G⁵¹ 4432 R⁶⁴ G⁵² 4433 R⁶⁵ G⁴⁹ 4434 R⁶⁵ G⁵⁰ 4435 R⁶⁵ G⁵¹ 4436 R⁶⁵ G⁵² 4437 R⁶⁶ G⁴⁹ 4438 R⁶⁶ G⁵⁰ 4439 R⁶⁶ G⁵¹ 4440 R⁶⁶ G⁵² 4441 R⁶⁷ G⁴⁹ 4442 R⁶⁷ G⁵⁰ 4443 R⁶⁷ G⁵¹ 4444 R⁶⁷ G⁵² 4445 R⁶⁸ G⁴⁹ 4446 R⁶⁸ G⁵⁰ 4447 R⁶⁸ G⁵¹ 4448 R⁶⁸ G⁵² 4449 R⁶⁹ G⁴⁹ 4450 R⁶⁹ G⁵⁰ 4451 R⁶⁹ G⁵¹ 4452 R⁶⁹ G⁵² 4453 R⁷⁰ G⁴⁹ 4454 R⁷⁰ G⁵⁰ 4455 R⁷⁰ G⁵¹ 4456 R⁷⁰ G⁵² 4457 R⁷¹ G⁴⁹ 4458 R⁷¹ G⁵⁰ 4459 R⁷¹ G⁵¹ 4460 R⁷¹ G⁵² 4461 R⁷² G⁴⁹ 4462 R⁷² G⁵⁰ 4463 R⁷² G⁵¹ 4464 R⁷² G⁵² 4465 R⁷³ G⁴⁹ 4466 R⁷³ G⁵⁰ 4467 R⁷³ G⁵¹ 4468 R⁷³ G⁵² 4469 R⁷⁴ G⁴⁹ 4470 R⁷⁴ G⁵⁰ 4471 R⁷⁴ G⁵¹ 4472 R⁷⁴ G⁵² 4473 R⁷⁵ G⁴⁹ 4474 R⁷⁵ G⁵⁰ 4475 R⁷⁵ G⁵¹ 4476 R⁷⁵ G⁵² 4477 R⁷⁶ G⁴⁹ 4478 R⁷⁶ G⁵⁰ 4479 R⁷⁶ G⁵¹ 4480 R⁷⁶ G⁵² 4481 R⁷⁷ G⁴⁹ 4482 R⁷⁷ G⁵⁰ 4483 R⁷⁷ G⁵¹ 4484 R⁷⁷ G⁵² 4485 R⁷⁸ G⁴⁹ 4486 R⁷⁸ G⁵⁰ 4487 R⁷⁸ G⁵¹ 4488 R⁷⁸ G⁵² 4489 R⁷⁹ G⁴⁹ 4490 R⁷⁹ G⁵⁰ 4491 R⁷⁹ G⁵¹ 4492 R⁷⁹ G⁵² 4493 R⁸⁰ G⁴⁹ 4494 R⁸⁰ G⁵⁰ 4495 R⁸⁰ G⁵¹ 4496 R⁸⁰ G⁵² 4497 R⁸¹ G⁴⁹ 4498 R⁸¹ G⁵⁰ 4499 R⁸¹ G⁵¹ 4500 R⁸¹ G⁵² 4501 R⁸² G⁴⁹ 4502 R⁸² G⁵⁰ 4503 R⁸² G⁵¹ 4504 R⁸² G⁵² 4505 R⁸³ G⁴⁹ 4506 R⁸³ G⁵⁰ 4507 R⁸³ G⁵¹ 4508 R⁸³ G⁵² 4509 R⁸⁴ G⁴⁹ 4510 R⁸⁴ G⁵⁰ 4511 R⁸⁴ G⁵¹ 4512 R⁸⁴ G⁵² 4513 R⁸⁵ G⁴⁹ 4514 R⁸⁵ G⁵⁰ 4515 R⁸⁵ G⁵¹ 4516 R⁸⁵ G⁵² 4517 R⁸⁶ G⁴⁹ 4518 R⁸⁶ G⁵⁰ 4519 R⁸⁶ G⁵¹ 4520 R⁸⁶ G⁵² 4521 R⁸⁷ G⁴⁹ 4522 R⁸⁷ G⁵⁰ 4523 R⁸⁷ G⁵¹ 4524 R⁸⁷ G⁵²;

wherein R¹ to R⁸⁷ have the following structures:

and wherein G¹ to G⁵² have the following structures:


11. The compound of claim 1, wherein the compound has a formula of M(L_(A))_(p)(L_(B))_(q)(L_(C))_(r) wherein L_(B) and L_(C) are each a bidentate ligand; and wherein p is 1, 2, or 3; q is 0, 1, or 2; r is 0, 1, or 2; and p+q+r is the oxidation state of the metal M.
 12. The compound of claim 11, wherein the compound has a formula selected from the group consisting of Ir(L_(A))₃, Ir(L_(A))(L_(B))₂, Ir(L_(A))₂(L_(B)), Ir(L_(A))₂(L_(C)), and Ir(L_(A))(L_(B))(L_(C)); and wherein L_(A), L_(B), and L_(C) are different from each other; or a formula of Pt(L_(A))(L_(B)); and wherein L_(A) and L_(B) can be same or different.
 13. The compound of claim 11, wherein L_(B) and L_(C) are each independently selected from the group consisting of:

wherein: T is selected from the group consisting of B, Al, Ga, and In; each of Y¹ to Y¹³ is independently selected from the group consisting of carbon and nitrogen; Y′ is selected from the group consisting of BR_(e), BR_(e)R_(f), NR_(e), PR_(e), P(O)R_(e), O, S, Se, C═O, C═S, C═Se, C═NR_(e), C═CR_(e)R_(f), S═O, SO₂, CR_(e)R_(f), SiR_(e)R_(f), and GeR_(e)R_(f); R_(e) and R_(f) can be fused or joined to form a ring; each R_(a), R_(b), R_(c), and R_(d) independently represent zero, mono, or up to a maximum allowed number of substitutions to its associated ring; each of R_(a1), R_(b1), R_(c1), R_(d1), R_(a), R_(b), R_(c), R_(d), R_(e) and R_(f) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halide, alkyl, cycloalkyl, heteroalkyl, arylalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carbonyl, carboxylic acid, ester, nitrile, isonitrile, sulfanyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; the general substituents defined herein; and any two adjacent R_(a), R_(b), R_(c), R_(d), R_(e) and R_(f) can be fused or joined to form a ring or form a multidentate ligand.
 14. The compound of claim 10, wherein when the compound has formula Ir(L_(A-i-m-X))₃, i is an integer from 1 to 4524; m is an integer from 1 to 184; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₃ to Ir(L_(A4524-184-4))₃; when the compound has formula Ir(L_(Ai-m-X))(L_(Bk))₂, i is an integer from 1 to 4524; m is an integer from 1 to 184; k is an integer from 1 to 324; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))(L_(B1))₂ to Ir(L_(A4524-184-4))(L_(B324))₂; when the compound has formula Ir(L_(Ai-m-X))₂(L_(Bk)), i is an integer from 1 to 4524; m is an integer from 1 to 184; k is an integer from 1 to 324; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(B1)) to Ir(L_(A4524-184-4))₂(L_(B324)); when the compound has formula Ir(L_(Ai-m-X))₂(L_(Cj-I)), i is an integer from 1 to 4524; m is an integer from 1 to 184; j is an integer from 1 to 1416; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(C1-I)) to Ir(L_(A4524-184-4))₂(L_(C1416-I)); and when the compound has formula Ir(L_(Ai-m-X))₂(L_(Cj-II)), i is an integer from 1 to 4524; m is an integer from 1 to 184; j is an integer from 1 to 1416; X is an integer from 1 to 4; and the compound is selected from the group consisting of Ir(L_(A1-1-1))₂(L_(C1-II)) to Ir(L_(A4524-184-4))₂(L_(C1416-II)); wherein each L_(Bk) has the structure defined as follows:

wherein each L_(Cj-I) has a structure based on formula

and each L_(Cj-II) has a structure based on formula

wherein for each L_(Cj) in L_(Cj-I) and L_(Cj-II), R²⁰¹ and R²⁰² are each independently defined as follows: L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(Cj) R²⁰¹ R²⁰² L_(C1) R^(D1) R^(D1) L_(C193) R^(D1) R^(D3) L_(C385) R^(D17) R^(D40) L_(C577) R^(D143) R^(D120) L_(C2) R^(D2) R^(D2) L_(C194) R^(D1) R^(D4) L_(C386) R^(D17) R^(D41) L_(C578) R^(D143) R^(D133) L_(C3) R^(D3) R^(D3) L_(C195) R^(D1) R^(D5) L_(C387) R^(D17) R^(D42) L_(C579) R^(D143) R^(D134) L_(C4) R^(D4) R^(D4) L_(C196) R^(D1) R^(D9) L_(C388) R^(D17) R^(D43) L_(C580) R^(D143) R^(D135) L_(C5) R^(D5) R^(D5) L_(C197) R^(D1) R^(D10) L_(C389) R^(D17) R^(D48) L_(C581) R^(D143) R^(D136) L_(C6) R^(D6) R^(D6) L_(C198) R^(D1) R^(D17) L_(C390) R^(D17) R^(D49) L_(C582) R^(D143) R^(D144) L_(C7) R^(D7) R^(D7) L_(C199) R^(D1) R^(D18) L_(C391) R^(D17) R^(D50) L_(C583) R^(D143) R^(D145) L_(C8) R^(D8) R^(D8) L_(C200) R^(D1) R^(D20) L_(C392) R^(D17) R^(D54) L_(C584) R^(D143) R^(D146) L_(C9) R^(D9) R^(D9) L_(C201) R^(D1) R^(D22) L_(C393) R^(D17) R^(D55) L_(C585) R^(D143) R^(D147) L_(C10) R^(D10) R^(D10) L_(C202) R^(D1) R^(D37) L_(C394) R^(D17) R^(D58) L_(C586) R^(D143) R^(D149) L_(C11) R^(D11) R^(D11) L_(C203) R^(D1) R^(D40) L_(C395) R^(D17) R^(D59) L_(C587) R^(D143) R^(D151) L_(C12) R^(D12) R^(D12) L_(C204) R^(D1) R^(D41) L_(C396) R^(D17) R^(D78) L_(C588) R^(D143) R^(D154) L_(C13) R^(D13) R^(D13) L_(C205) R^(D1) R^(D42) L_(C397) R^(D17) R^(D79) L_(C589) R^(D143) R^(D155) L_(C14) R^(D14) R^(D14) L_(C206) R^(D1) R^(D43) L_(C398) R^(D17) R^(D81) L_(C590) R^(D143) R^(D161) L_(C15) R^(D15) R^(D15) L_(C207) R^(D1) R^(D48) L_(C399) R^(D17) R^(D87) L_(C591) R^(D143) R^(D175) L_(C16) R^(D16) R^(D16) L_(C208) R^(D1) R^(D49) L_(C400) R^(D17) R^(D88) L_(C592) R^(D144) R^(D3) L_(C17) R^(D17) R^(D17) L_(C209) R^(D1) R^(D50) L_(C401) R^(D17) R^(D89) L_(C593) R^(D144) R^(D5) L_(C18) R^(D18) R^(D18) L_(C210) R^(D1) R^(D54) L_(C402) R^(D17) R^(D93) L_(C594) R^(D144) R^(D17) L_(C19) R^(D19) R^(D19) L_(C211) R^(D1) R^(D55) L_(C403) R^(D17) R^(D116) L_(C595) R^(D144) R^(D18) L_(C20) R^(D20) R^(D20) L_(C212) R^(D1) R^(D5S) L_(C404) R^(D17) R^(D117) L_(C596) R^(D144) R^(D20) L_(C21) R^(D21) R^(D21) L_(C213) R^(D1) R^(D59) L_(C405) R^(D17) R^(D118) L_(C597) R^(D144) R^(D22) L_(C22) R^(D22) R^(D22) L_(C214) R^(D1) R^(D78) L_(C406) R^(D17) R^(D119) L_(C598) R^(D144) R^(D37) L_(C23) R^(D23) R^(D23) L_(C215) R^(D1) R^(D79) L_(C407) R^(D17) R^(D120) L_(C599) R^(D144) R^(D40) L_(C24) R^(D24) R^(D24) L_(C216) R^(D1) R^(D81) L_(C408) R^(D17) R^(D133) L_(C600) R^(D144) R^(D41) L_(C25) R^(D25) R^(D25) L_(C217) R^(D1) R^(D87) L_(C409) R^(D17) R^(D134) L_(C601) R^(D144) R^(D42) L_(C26) R^(D26) R^(D26) L_(C218) R^(D1) R^(D88) L_(C410) R^(D17) R^(D135) L_(C602) R^(D144) R^(D43) L_(C27) R^(D27) R^(D27) L_(C219) R^(D1) R^(D89) L_(C411) R^(D17) R^(D136) L_(C603) R^(D144) R^(D48) L_(C28) R^(D28) R^(D28) L_(C220) R^(D1) R^(D93) L_(C412) R^(D17) R^(D143) L_(C604) R^(D144) R^(D49) L_(C29) R^(D29) R^(D29) L_(C221) R^(D1) R^(D116) L_(C413) R^(D17) R^(D144) L_(C605) R^(D144) R^(D54) L_(C30) R^(D30) R^(D30) L_(C222) R^(D1) R^(D117) L_(C414) R^(D17) R^(D145) L_(C606) R^(D144) R^(D58) L_(C31) R^(D31) R^(D31) L_(C223) R^(D1) R^(D118) L_(C415) R^(D17) R^(D146) L_(C607) R^(D144) R^(D59) L_(C32) R^(D32) R^(D32) L_(C224) R^(D1) R^(D119) L_(C416) R^(D17) R^(D147) L_(C608) R^(D144) R^(D78) L_(C33) R^(D33) R^(D33) L_(C225) R^(D1) R^(D120) L_(C417) R^(D17) R^(D149) L_(C609) R^(D144) R^(D79) L_(C34) R^(D34) R^(D34) L_(C226) R^(D1) R^(D133) L_(C418) R^(D17) R^(D151) L_(C610) R^(D144) R^(D81) L_(C35) R^(D35) R^(D35) L_(C227) R^(D1) R^(D134) L_(C419) R^(D17) R^(D154) L_(C611) R^(D144) R^(D87) L_(C36) R^(D36) R^(D36) L_(C228) R^(D1) R^(D135) L_(C420) R^(D17) R^(D155) L_(C612) R^(D144) R^(D88) L_(C37) R^(D37) R^(D37) L_(C229) R^(D1) R^(D136) L_(C421) R^(D17) R^(D161) L_(C613) R^(D144) R^(D89) L_(C38) R^(D38) R^(D38) L_(C230) R^(D1) R^(D143) L_(C422) R^(D17) R^(D175) L_(C614) R^(D144) R^(D93) L_(C39) R^(D39) R^(D39) L_(C231) R^(D1) R^(D144) L_(C423) R^(D50) R^(D3) L_(C615) R^(D144) R^(D116) L_(C40) R^(D40) R^(D40) L_(C232) R^(D1) R^(D145) L_(C424) R^(D50) R^(D5) L_(C616) R^(D144) R^(D117) L_(C41) R^(D41) R^(D41) L_(C233) R^(D1) R^(D146) L_(C425) R^(D50) R^(D18) L_(C617) R^(D144) R^(D118) L_(C42) R^(D42) R^(D42) L_(C234) R^(D1) R^(D147) L_(C426) R^(D50) R^(D20) L_(C618) R^(D144) R^(D119) L_(C43) R^(D43) R^(D43) L_(C235) R^(D1) R^(D149) L_(C427) R^(D50) R^(D22) L_(C619) R^(D144) R^(D120) L_(C44) R^(D44) R^(D44) L_(C236) R^(D1) R^(D151) L_(C428) R^(D50) R^(D37) L_(C620) R^(D144) R^(D133) L_(C45) R^(D45) R^(D45) L_(C237) R^(D1) R^(D154) L_(C429) R^(D50) R^(D40) L_(C621) R^(D144) R^(D134) L_(C46) R^(D46) R^(D46) L_(C238) R^(D1) R^(D155) L_(C430) R^(D50) R^(D41) L_(C622) R^(D144) R^(D135) L_(C47) R^(D47) R^(D47) L_(C239) R^(D1) R^(D161) L_(C431) R^(D50) R^(D42) L_(C623) R^(D144) R^(D136) L_(C48) R^(D48) R^(D48) L_(C240) R^(D1) R^(D175) L_(C432) R^(D50) R^(D43) L_(C624) R^(D144) R^(D145) L_(C49) R^(D49) R^(D49) L_(C241) R^(D4) R^(D3) L_(C433) R^(D50) R^(D48) L_(C625) R^(D144) R^(D146) L_(C50) R^(D50) R^(D50) L_(C242) R^(D4) R^(D5) L_(C434) R^(D50) R^(D49) L_(C626) R^(D144) R^(D147) L_(C51) R^(D51) R^(D51) L_(C243) R^(D4) R^(D9) L_(C435) R^(D50) R^(D54) L_(C627) R^(D144) R^(D149) L_(C52) R^(D52) R^(D52) L_(C244) R^(D4) R^(D10) L_(C436) R^(D50) R^(D55) L_(C628) R^(D144) R^(D151) L_(C53) R^(D53) R^(D53) L_(C245) R^(D4) R^(D17) L_(C437) R^(D50) R^(D58) L_(C629) R^(D144) R^(D154) L_(C54) R^(D54) R^(D54) L_(C246) R^(D4) R^(D18) L_(C438) R^(D50) R^(D59) L_(C630) R^(D144) R^(D155) L_(C55) R^(D55) R^(D55) L_(C247) R^(D4) R^(D20) L_(C439) R^(D50) R^(D78) L_(C631) R^(D144) R^(D161) L_(C56) R^(D56) R^(D56) L_(C248) R^(D4) R^(D22) L_(C440) R^(D50) R^(D79) L_(C632) R^(D144) R^(D175) L_(C57) R^(D57) R^(D57) L_(C249) R^(D4) R^(D37) L_(C441) R^(D50) R^(D81) L_(C633) R^(D145) R^(D3) L_(C58) R^(D58) R^(D58) L_(C250) R^(D4) R^(D40) L_(C442) R^(D50) R^(D87) L_(C634) R^(D145) R^(D5) L_(C59) R^(D59) R^(D59) L_(C251) R^(D4) R^(D41) L_(C443) R^(D50) R^(D88) L_(C635) R^(D145) R^(D17) L_(C60) R^(D60) R^(D60) L_(C252) R^(D4) R^(D42) L_(C444) R^(D50) R^(D89) L_(C636) R^(D145) R^(D18) L_(C61) R^(D61) R^(D61) L_(C253) R^(D4) R^(D43) L_(C445) R^(D50) R^(D93) L_(C637) R^(D145) R^(D20) L_(C62) R^(D62) R^(D62) L_(C254) R^(D4) R^(D48) L_(C446) R^(D50) R^(D116) L_(C638) R^(D145) R^(D22) L_(C63) R^(D63) R^(D63) L_(C255) R^(D4) R^(D49) L_(C447) R^(D50) R^(D117) L_(C639) R^(D145) R^(D37) L_(C64) R^(D64) R^(D64) L_(C256) R^(D4) R^(D50) L_(C448) R^(D50) R^(D118) L_(C640) R^(D145) R^(D40) L_(C65) R^(D65) R^(D65) L_(C257) R^(D4) R^(D54) L_(C449) R^(D50) R^(D119) L_(C641) R^(D145) R^(D41) L_(C66) R^(D66) R^(D66) L_(C258) R^(D4) R^(D55) L_(C450) R^(D50) R^(D120) L_(C642) R^(D145) R^(D42) L_(C67) R^(D67) R^(D67) L_(C259) R^(D4) R^(D58) L_(C451) R^(D50) R^(D133) L_(C643) R^(D145) R^(D43) L_(C68) R^(D68) R^(D68) L_(C260) R^(D4) R^(D59) L_(C452) R^(D50) R^(D134) L_(C644) R^(D145) R^(D48) L_(C69) R^(D69) R^(D69) L_(C261) R^(D4) R^(D78) L_(C453) R^(D50) R^(D135) L_(C645) R^(D145) R^(D49) L_(C70) R^(D70) R^(D70) L_(C262) R^(D4) R^(D79) L_(C454) R^(D50) R^(D136) L_(C646) R^(D145) R^(D54) L_(C71) R^(D71) R^(D71) L_(C263) R^(D4) R^(D81) L_(C455) R^(D50) R^(D143) L_(C647) R^(D145) R^(D58) L_(C72) R^(D72) R^(D72) L_(C264) R^(D4) R^(D87) L_(C456) R^(D50) R^(D144) L_(C648) R^(D145) R^(D59) L_(C73) R^(D73) R^(D73) L_(C265) R^(D4) R^(D88) L_(C457) R^(D50) R^(D145) L_(C649) R^(D145) R^(D78) L_(C74) R^(D74) R^(D74) L_(C266) R^(D4) R^(D89) L_(C458) R^(D50) R^(D146) L_(C650) R^(D145) R^(D79) L_(C75) R^(D75) R^(D75) L_(C267) R^(D4) R^(D93) L_(C459) R^(D50) R^(D147) L_(C651) R^(D145) R^(D81) L_(C76) R^(D76) R^(D76) L_(C268) R^(D4) R^(D116) L_(C460) R^(D50) R^(D149) L_(C652) R^(D145) R^(D87) L_(C77) R^(D77) R^(D77) L_(C269) R^(D4) R^(D117) L_(C461) R^(D50) R^(D151) L_(C653) R^(D145) R^(D88) L_(C78) R^(D78) R^(D78) L_(C270) R^(D4) R^(D118) L_(C462) R^(D50) R^(D154) L_(C654) R^(D145) R^(D89) L_(C79) R^(D79) R^(D79) L_(C271) R^(D4) R^(D119) L_(C463) R^(D50) R^(D155) L_(C655) R^(D145) R^(D93) L_(C80) R^(D80) R^(D80) L_(C272) R^(D4) R^(D120) L_(C464) R^(D50) R^(D161) L_(C656) R^(D145) R^(D116) L_(C81) R^(D81) R^(D81) L_(C273) R^(D4) R^(D133) L_(C465) R^(D50) R^(D175) L_(C657) R^(D145) R^(D117) L_(C82) R^(D82) R^(D82) L_(C274) R^(D4) R^(D134) L_(C466) R^(D55) R^(D3) L_(C658) R^(D145) R^(D118) L_(C83) R^(D83) R^(D83) L_(C275) R^(D4) R^(D135) L_(C467) R^(D55) R^(D5) L_(C659) R^(D145) R^(D119) L_(C84) R^(D84) R^(D84) L_(C276) R^(D4) R^(D136) L_(C468) R^(D55) R^(D18) L_(C660) R^(D145) R^(D120) L_(C85) R^(D85) R^(D85) L_(C277) R^(D4) R^(D143) L_(C469) R^(D55) R^(D20) L_(C661) R^(D145) R^(D133) L_(C86) R^(D86) R^(D86) L_(C278) R^(D4) R^(D144) L_(C470) R^(D55) R^(D22) L_(C662) R^(D145) R^(D134) L_(C87) R^(D87) R^(D87) L_(C279) R^(D4) R^(D145) L_(C471) R^(D55) R^(D37) L_(C663) R^(D145) R^(D135) L_(C88) R^(D88) R^(D88) L_(C280) R^(D4) R^(D146) L_(C472) R^(D55) R^(D40) L_(C664) R^(D145) R^(D136) L_(C89) R^(D89) R^(D89) L_(C281) R^(D4) R^(D147) L_(C473) R^(D55) R^(D41) L_(C665) R^(D145) R^(D146) L_(C90) R^(D90) R^(D90) L_(C282) R^(D4) R^(D149) L_(C474) R^(D55) R^(D42) L_(C666) R^(D145) R^(D147) L_(C91) R^(D91) R^(D91) L_(C283) R^(D4) R^(D151) L_(C475) R^(D55) R^(D43) L_(C667) R^(D145) R^(D149) L_(C92) R^(D92) R^(D92) L_(C284) R^(D4) R^(D154) L_(C476) R^(D55) R^(D48) L_(C668) R^(D145) R^(D151) L_(C93) R^(D93) R^(D93) L_(C285) R^(D4) R^(D155) L_(C477) R^(D55) R^(D49) L_(C669) R^(D145) R^(D154) L_(C94) R^(D94) R^(D94) L_(C286) R^(D4) R^(D161) L_(C478) R^(D55) R^(D54) L_(C670) R^(D145) R^(D155) L_(C95) R^(D95) R^(D95) L_(C287) R^(D4) R^(D175) L_(C479) R^(D55) R^(D58) L_(C671) R^(D145) R^(D161) L_(C96) R^(D96) R^(D96) L_(C288) R^(D9) R^(D3) L_(C480) R^(D55) R^(D59) L_(C672) R^(D145) R^(D175) L_(C97) R^(D97) R^(D97) L_(C289) R^(D9) R^(D5) L_(C481) R^(D55) R^(D78) L_(C673) R^(D146) R^(D3) L_(C98) R^(D98) R^(D98) L_(C290) R^(D9) R^(D10) L_(C482) R^(D55) R^(D79) L_(C674) R^(D146) R^(D5) L_(C99) R^(D99) R^(D99) L_(C291) R^(D9) R^(D17) L_(C483) R^(D55) R^(D81) L_(C675) R^(D146) R^(D17) L_(C100) R^(D100) R^(D100) L_(C292) R^(D9) R^(D18) L_(C484) R^(D55) R^(D87) L_(C676) R^(D146) R^(D18) L_(C101) R^(D101) R^(D101) L_(C293) R^(D9) R^(D20) L_(C485) R^(D55) R^(D88) L_(C677) R^(D146) R^(D20) L_(C102) R^(D102) R^(D102) L_(C294) R^(D9) R^(D22) L_(C486) R^(D55) R^(D89) L_(C678) R^(D146) R^(D22) L_(C103) R^(D103) R^(D103) L_(C295) R^(D9) R^(D37) L_(C487) R^(D55) R^(D93) L_(C679) R^(D146) R^(D37) L_(C104) R^(D104) R^(D104) L_(C296) R^(D9) R^(D40) L_(C488) R^(D55) R^(D116) L_(C680) R^(D146) R^(D40) L_(C105) R^(D105) R^(D105) L_(C297) R^(D9) R^(D41) L_(C489) R^(D55) R^(D117) L_(C681) R^(D146) R^(D41) L_(C106) R^(D106) R^(D106) L_(C298) R^(D9) R^(D42) L_(C490) R^(D55) R^(D118) L_(C682) R^(D146) R^(D42) L_(C107) R^(D107) R^(D107) L_(C299) R^(D9) R^(D43) L_(C491) R^(D55) R^(D119) L_(C683) R^(D146) R^(D43) L_(C108) R^(D108) R^(D108) L_(C300) R^(D9) R^(D48) L_(C492) R^(D55) R^(D120) L_(C684) R^(D146) R^(D48) L_(C109) R^(D109) R^(D109) L_(C301) R^(D9) R^(D49) L_(C493) R^(D55) R^(D133) L_(C685) R^(D146) R^(D49) L_(C110) R^(D110) R^(D110) L_(C302) R^(D9) R^(D50) L_(C494) R^(D55) R^(D134) L_(C686) R^(D146) R^(D54) L_(C111) R^(D111) R^(D111) L_(C303) R^(D9) R^(D54) L_(C495) R^(D55) R^(D135) L_(C687) R^(D146) R^(D58) L_(C112) R^(D112) R^(D112) L_(C304) R^(D9) R^(D55) L_(C496) R^(D55) R^(D136) L_(C688) R^(D146) R^(D59) L_(C113) R^(D113) R^(D113) L_(C305) R^(D9) R^(D58) L_(C497) R^(D55) R^(D143) L_(C689) R^(D146) R^(D78) L_(C114) R^(D114) R^(D114) L_(C306) R^(D9) R^(D59) L_(C498) R^(D55) R^(D144) L_(C690) R^(D146) R^(D79) L_(C115) R^(D115) R^(D115) L_(C307) R^(D9) R^(D78) L_(C499) R^(D55) R^(D145) L_(C691) R^(D146) R^(D81) L_(C116) R^(D116) R^(D116) L_(C308) R^(D9) R^(D79) L_(C500) R^(D55) R^(D146) L_(C692) R^(D146) R^(D87) L_(C117) R^(D117) R^(D117) L_(C309) R^(D9) R^(D81) L_(C501) R^(D55) R^(D147) L_(C693) R^(D146) R^(D88) L_(C118) R^(D118) R^(D118) L_(C310) R^(D9) R^(D87) L_(C502) R^(D55) R^(D149) L_(C694) R^(D146) R^(D89) L_(C119) R^(D119) R^(D119) L_(C311) R^(D9) R^(D88) L_(C503) R^(D55) R^(D151) L_(C695) R^(D146) R^(D93) L_(C120) R^(D120) R^(D120) L_(C312) R^(D9) R^(D89) L_(C504) R^(D55) R^(D154) L_(C696) R^(D146) R^(D117) L_(C121) R^(D121) R^(D121) L_(C313) R^(D9) R^(D95) L_(C505) R^(D55) R^(D155) L_(C697) R^(D146) R^(D118) L_(C122) R^(D122) R^(D122) L_(C314) R^(D9) R^(D116) L_(C506) R^(D55) R^(D161) L_(C698) R^(D146) R^(D119) L_(C123) R^(D123) R^(D123) L_(C315) R^(D9) R^(D117) L_(C507) R^(D55) R^(D175) L_(C699) R^(D146) R^(D120) L_(C124) R^(D124) R^(D124) L_(C316) R^(D9) R^(D118) L_(C508) R^(D116) R^(D3) L_(C700) R^(D146) R^(D133) L_(C125) R^(D125) R^(D125) L_(C317) R^(D9) R^(D119) L_(C509) R^(D116) R^(D5) L_(C701) R^(D146) R^(D134) L_(C126) R^(D126) R^(D126) L_(C318) R^(D9) R^(D120) L_(C510) R^(D116) R^(D17) L_(C702) R^(D146) R^(D135) L_(C127) R^(D127) R^(D127) L_(C319) R^(D9) R^(D133) L_(C511) R^(D116) R^(D18) L_(C703) R^(D146) R^(D136) L_(C128) R^(D128) R^(D128) L_(C320) R^(D9) R^(D134) L_(C512) R^(D116) R^(D20) L_(C704) R^(D146) R^(D146) L_(C129) R^(D129) R^(D129) L_(C321) R^(D9) R^(D135) L_(C513) R^(D116) R^(D22) L_(C705) R^(D146) R^(D147) L_(C130) R^(D130) R^(D130) L_(C322) R^(D9) R^(D136) L_(C514) R^(D116) R^(D37) L_(C706) R^(D146) R^(D149) L_(C131) R^(D131) R^(D131) L_(C323) R^(D9) R^(D143) L_(C515) R^(D116) R^(D40) L_(C707) R^(D146) R^(D151) L_(C132) R^(D132) R^(D132) L_(C324) R^(D9) R^(D144) L_(C516) R^(D116) R^(D41) L_(C708) R^(D146) R^(D154) L_(C133) R^(D133) R^(D133) L_(C325) R^(D9) R^(D145) L_(C517) R^(D116) R^(D42) L_(C709) R^(D146) R^(D155) L_(C134) R^(D134) R^(D134) L_(C326) R^(D9) R^(D146) L_(C518) R^(D116) R^(D43) L_(C710) R^(D146) R^(D161) L_(C135) R^(D135) R^(D135) L_(C327) R^(D9) R^(D147) L_(C519) R^(D116) R^(D48) L_(C711) R^(D146) R^(D175) L_(C136) R^(D136) R^(D136) L_(C328) R^(D9) R^(D149) L_(C520) R^(D116) R^(D49) L_(C712) R^(D133) R^(D3) L_(C137) R^(D137) R^(D137) L_(C329) R^(D9) R^(D151) L_(C521) R^(D116) R^(D54) L_(C713) R^(D133) R^(D5) L_(C138) R^(D138) R^(D138) L_(C330) R^(D9) R^(D154) L_(C522) R^(D116) R^(D58) L_(C714) R^(D133) R^(D3) L_(C139) R^(D139) R^(D139) L_(C331) R^(D9) R^(D155) L_(C523) R^(D116) R^(D59) L_(C715) R^(D133) R^(D18) L_(C140) R^(D140) R^(D140) L_(C332) R^(D9) R^(D161) L_(C524) R^(D116) R^(D78) L_(C716) R^(D133) R^(D20) L_(C141) R^(D141) R^(D141) L_(C333) R^(D9) R^(D175) L_(C525) R^(D116) R^(D79) L_(C717) R^(D133) R^(D22) L_(C142) R^(D142) R^(D142) L_(C334) R^(D10) R^(D3) L_(C526) R^(D116) R^(D81) L_(C718) R^(D133) R^(D37) L_(C143) R^(D143) R^(D143) L_(C335) R^(D10) R^(D5) L_(C527) R^(D116) R^(D87) L_(C719) R^(D133) R^(D40) L_(C144) R^(D144) R^(D144) L_(C336) R^(D10) R^(D17) L_(C528) R^(D116) R^(D88) L_(C720) R^(D133) R^(D41) L_(C145) R^(D145) R^(D145) L_(C337) R^(D10) R^(D18) L_(C529) R^(D116) R^(D89) L_(C721) R^(D133) R^(D42) L_(C146) R^(D146) R^(D146) L_(C338) R^(D10) R^(D20) L_(C530) R^(D116) R^(D93) L_(C722) R^(D133) R^(D43) L_(C147) R^(D147) R^(D147) L_(C339) R^(D10) R^(D22) L_(C531) R^(D116) R^(D117) L_(C723) R^(D133) R^(D48) L_(C148) R^(D148) R^(D148) L_(C340) R^(D10) R^(D37) L_(C532) R^(D116) R^(D118) L_(C724) R^(D133) R^(D49) L_(C149) R^(D149) R^(D149) L_(C341) R^(D10) R^(D40) L_(C533) R^(D116) R^(D119) L_(C725) R^(D133) R^(D54) L_(C150) R^(D150) R^(D150) L_(C342) R^(D10) R^(D41) L_(C534) R^(D116) R^(D120) L_(C726) R^(D133) R^(D58) L_(C151) R^(D151) R^(D151) L_(C343) R^(D10) R^(D42) L_(C535) R^(D116) R^(D133) L_(C727) R^(D133) R^(D59) L_(C152) R^(D152) R^(D152) L_(C344) R^(D10) R^(D43) L_(C536) R^(D116) R^(D134) L_(C728) R^(D133) R^(D78) L_(C153) R^(D153) R^(D153) L_(C345) R^(D10) R^(D48) L_(C537) R^(D116) R^(D135) L_(C729) R^(D133) R^(D79) L_(C154) R^(D154) R^(D154) L_(C346) R^(D10) R^(D49) L_(C538) R^(D116) R^(D136) L_(C730) R^(D133) R^(D81) L_(C155) R^(D155) R^(D155) L_(C347) R^(D10) R^(D50) L_(C539) R^(D116) R^(D143) L_(C731) R^(D133) R^(D87) L_(C156) R^(D156) R^(D156) L_(C348) R^(D10) R^(D54) L_(C540) R^(D116) R^(D144) L_(C732) R^(D133) R^(D88) L_(C157) R^(D157) R^(D157) L_(C349) R^(D10) R^(D55) L_(C541) R^(D116) R^(D145) L_(C733) R^(D133) R^(D89) L_(C158) R^(D158) R^(D158) L_(C350) R^(D10) R^(D58) L_(C542) R^(D116) R^(D146) L_(C734) R^(D133) R^(D93) L_(C159) R^(D159) R^(D159) L_(C351) R^(D10) R^(D59) L_(C543) R^(D116) R^(D147) L_(C735) R^(D133) R^(D117) L_(C160) R^(D160) R^(D160) L_(C352) R^(D10) R^(D78) L_(C544) R^(D116) R^(D149) L_(C736) R^(D133) R^(D118) L_(C161) R^(D161) R^(D161) L_(C353) R^(D10) R^(D79) L_(C545) R^(D116) R^(D151) L_(C737) R^(D133) R^(D119) L_(C162) R^(D162) R^(D162) L_(C354) R^(D10) R^(D81) L_(C546) R^(D116) R^(D154) L_(C738) R^(D133) R^(D120) L_(C163) R^(D163) R^(D163) L_(C355) R^(D10) R^(D87) L_(C547) R^(D116) R^(D155) L_(C739) R^(D133) R^(D133) L_(C164) R^(D164) R^(D164) L_(C356) R^(D10) R^(D88) L_(C548) R^(D116) R^(D161) L_(C740) R^(D133) R^(D134) L_(C165) R^(D165) R^(D165) L_(C357) R^(D10) R^(D89) L_(C549) R^(D116) R^(D175) L_(C741) R^(D133) R^(D135) L_(C166) R^(D166) R^(D166) L_(C358) R^(D10) R^(D93) L_(C550) R^(D143) R^(D3) L_(C742) R^(D133) R^(D136) L_(C167) R^(D167) R^(D167) L_(C359) R^(D10) R^(D116) L_(C551) R^(D143) R^(D5) L_(C743) R^(D133) R^(D146) L_(C168) R^(D168) R^(D168) L_(C360) R^(D10) R^(D117) L_(C552) R^(D143) R^(D17) L_(C744) R^(D133) R^(D147) L_(C169) R^(D169) R^(D169) L_(C361) R^(D10) R^(D118) L_(C553) R^(D143) R^(D18) L_(C745) R^(D133) R^(D149) L_(C170) R^(D170) R^(D170) L_(C362) R^(D10) R^(D119) L_(C554) R^(D143) R^(D20) L_(C746) R^(D133) R^(D151) L_(C171) R^(D171) R^(D171) L_(C363) R^(D10) R^(D120) L_(C555) R^(D143) R^(D22) L_(C747) R^(D133) R^(D154) L_(C172) R^(D172) R^(D172) L_(C364) R^(D10) R^(D133) L_(C556) R^(D143) R^(D37) L_(C748) R^(D133) R^(D155) L_(C173) R^(D173) R^(D173) L_(C365) R^(D10) R^(D134) L_(C557) R^(D143) R^(D40) L_(C749) R^(D133) R^(D161) L_(C174) R^(D174) R^(D174) L_(C366) R^(D10) R^(D135) L_(C558) R^(D143) R^(D41) L_(C750) R^(D133) R^(D175) L_(C175) R^(D175) R^(D175) L_(C367) R^(D10) R^(D136) L_(C559) R^(D143) R^(D42) L_(C751) R^(D175) R^(D3) L_(C176) R^(D176) R^(D176) L_(C368) R^(D10) R^(D143) L_(C560) R^(D143) R^(D43) L_(C752) R^(D175) R^(D5) L_(C177) R^(D177) R^(D177) L_(C369) R^(D10) R^(D144) L_(C561) R^(D143) R^(D48) L_(C753) R^(D175) R^(D18) L_(C178) R^(D178) R^(D178) L_(C370) R^(D10) R^(D145) L_(C562) R^(D143) R^(D49) L_(C754) R^(D175) R^(D20) L_(C179) R^(D179) R^(D179) L_(C371) R^(D10) R^(D146) L_(C563) R^(D143) R^(D54) L_(C755) R^(D175) R^(D22) L_(C180) R^(D180) R^(D180) L_(C372) R^(D10) R^(D147) L_(C564) R^(D143) R^(D58) L_(C756) R^(D175) R^(D37) L_(C181) R^(D181) R^(D181) L_(C373) R^(D10) R^(D149) L_(C565) R^(D143) R^(D59) L_(C757) R^(D175) R^(D40) L_(C182) R^(D182) R^(D182) L_(C374) R^(D10) R^(D151) L_(C566) R^(D143) R^(D78) L_(C758) R^(D175) R^(D41) L_(C183) R^(D183) R^(D183) L_(C375) R^(D10) R^(D154) L_(C567) R^(D143) R^(D79) L_(C759) R^(D175) R^(D42) L_(C184) R^(D184) R^(D184) L_(C376) R^(D10) R^(D155) L_(C568) R^(D143) R^(D81) L_(C760) R^(D175) R^(D43) L_(C185) R^(D185) R^(D185) L_(C377) R^(D10) R^(D161) L_(C569) R^(D143) R^(D87) L_(C761) R^(D175) R^(D48) L_(C186) R^(D186) R^(D186) L_(C378) R^(D10) R^(D175) L_(C570) R^(D143) R^(D88) L_(C762) R^(D175) R^(D49) L_(C187) R^(D187) R^(D187) L_(C379) R^(D17) R^(D3) L_(C571) R^(D143) R^(D89) L_(C763) R^(D175) R^(D54) L_(C188) R^(D188) R^(D188) L_(C380) R^(D17) R^(D5) L_(C572) R^(D143) R^(D93) L_(C764) R^(D175) R^(D58) L_(C189) R^(D189) R^(D189) L_(C381) R^(D17) R^(D18) L_(C573) R^(D143) R^(D116) L_(C765) R^(D175) R^(D59) L_(C190) R^(D190) R^(D190) L_(C382) R^(D17) R^(D20) L_(C574) R^(D143) R^(D117) L_(C766) R^(D175) R^(D78) L_(C191) R^(D191) R^(D191) L_(C383) R^(D17) R^(D22) L_(C575) R^(D143) R^(D118) L_(C767) R^(D175) R^(D79) L_(C192) R^(D192) R^(D192) L_(C384) R^(D17) R^(D37) L_(C576) R^(D143) R^(D119) L_(C768) R^(D175) R^(D81) L_(C769) R^(D193) R^(D193) L_(C877) R^(D1) R^(D193) L_(C985) R^(D4) R^(D193) L_(C1093) R^(D9) R^(D193) L_(C770) R^(D194) R^(D194) L_(C878) R^(D1) R^(D194) L_(C986) R^(D4) R^(D194) L_(C1094) R^(D9) R^(D194) L_(C771) R^(D195) R^(D195) L_(C879) R^(D1) R^(D195) L_(C987) R^(D4) R^(D195) L_(C1095) R^(D9) R^(D195) L_(C772) R^(D196) R^(D196) L_(C880) R^(D1) R^(D196) L_(C988) R^(D4) R^(D196) L_(C1096) R^(D9) R^(D196) L_(C773) R^(D197) R^(D197) L_(C881) R^(D1) R^(D197) L_(C989) R^(D4) R^(D197) L_(C1097) R^(D9) R^(D197) L_(C774) R^(D198) R^(D198) L_(C882) R^(D1) R^(D198) L_(C990) R^(D4) R^(D198) L_(C1098) R^(D9) R^(D198) L_(C775) R^(D199) R^(D199) L_(C883) R^(D1) R^(D199) L_(C991) R^(D4) R^(D199) L_(C1099) R^(D9) R^(D199) L_(C776) R^(D200) R^(D200) L_(C884) R^(D1) R^(D200) L_(C992) R^(D4) R^(D200) L_(C1100) R^(D9) R^(D200) L_(C777) R^(D201) R^(D201) L_(C885) R^(D1) R^(D201) L_(C993) R^(D4) R^(D201) L_(C1101) R^(D9) R^(D201) L_(C778) R^(D202) R^(D202) L_(C886) R^(D1) R^(D202) L_(C994) R^(D4) R^(D202) L_(C1102) R^(D9) R^(D202) L_(C779) R^(D203) R^(D203) L_(C887) R^(D1) R^(D203) L_(C995) R^(D4) R^(D203) L_(C1103) R^(D9) R^(D203) L_(C780) R^(D204) R^(D204) L_(C888) R^(D1) R^(D204) L_(C996) R^(D4) R^(D204) L_(C1104) R^(D9) R^(D204) L_(C781) R^(D205) R^(D205) L_(C889) R^(D1) R^(D205) L_(C997) R^(D4) R^(D205) L_(C1105) R^(D9) R^(D205) L_(C782) R^(D206) R^(D206) L_(C890) R^(D1) R^(D206) L_(C998) R^(D4) R^(D206) L_(C1106) R^(D9) R^(D206) L_(C783) R^(D207) R^(D207) L_(C891) R^(D1) R^(D207) L_(C999) R^(D4) R^(D207) L_(C1107) R^(D9) R^(D207) L_(C784) R^(D208) R^(D208) L_(C892) R^(D1) R^(D208) L_(C1000) R^(D4) R^(D208) L_(C1108) R^(D9) R^(D208) L_(C785) R^(D209) R^(D209) L_(C893) R^(D1) R^(D209) L_(C1001) R^(D4) R^(D209) L_(C1109) R^(D9) R^(D209) L_(C786) R^(D210) R^(D210) L_(C894) R^(D1) R^(D210) L_(C1002) R^(D4) R^(D210) L_(C1110) R^(D9) R^(D210) L_(C787) R^(D211) R^(D211) L_(C895) R^(D1) R^(D211) L_(C1003) R^(D4) R^(D211) L_(C1111) R^(D9) R^(D211) L_(C788) R^(D212) R^(D212) L_(C896) R^(D1) R^(D212) L_(C1004) R^(D4) R^(D212) L_(C1112) R^(D9) R^(D212) L_(C789) R^(D213) R^(D213) L_(C897) R^(D1) R^(D213) L_(C1005) R^(D4) R^(D213) L_(C1113) R^(D9) R^(D213) L_(C790) R^(D214) R^(D214) L_(C898) R^(D1) R^(D214) L_(C1006) R^(D4) R^(D214) L_(C1114) R^(D9) R^(D214) L_(C791) R^(D215) R^(D215) L_(C899) R^(D1) R^(D215) L_(C1007) R^(D4) R^(D215) L_(C1115) R^(D9) R^(D215) L_(C792) R^(D216) R^(D216) L_(C900) R^(D1) R^(D216) L_(C1008) R^(D4) R^(D216) L_(C1116) R^(D9) R^(D216) L_(C793) R^(D217) R^(D217) L_(C901) R^(D1) R^(D217) L_(C1009) R^(D4) R^(D217) L_(C1117) R^(D9) R^(D217) L_(C794) R^(D218) R^(D218) L_(C902) R^(D1) R^(D218) L_(C1010) R^(D4) R^(D218) L_(C1118) R^(D9) R^(D218) L_(C795) R^(D219) R^(D219) L_(C903) R^(D1) R^(D219) L_(C1011) R^(D4) R^(D219) L_(C1119) R^(D9) R^(D219) L_(C796) R^(D220) R^(D220) L_(C904) R^(D1) R^(D220) L_(C1012) R^(D4) R^(D220) L_(C1120) R^(D9) R^(D220) L_(C797) R^(D221) R^(D221) L_(C905) R^(D1) R^(D221) L_(C1013) R^(D4) R^(D221) L_(C1121) R^(D9) R^(D221) L_(C798) R^(D222) R^(D222) L_(C906) R^(D1) R^(D222) L_(C1014) R^(D4) R^(D222) L_(C1122) R^(D9) R^(D222) L_(C799) R^(D223) R^(D223) L_(C907) R^(D1) R^(D223) L_(C1015) R^(D4) R^(D223) L_(C1123) R^(D9) R^(D223) L_(C800) R^(D224) R^(D224) L_(C908) R^(D1) R^(D224) L_(C1016) R^(D4) R^(D224) L_(C1124) R^(D9) R^(D224) L_(C801) R^(D225) R^(D225) L_(C909) R^(D1) R^(D225) L_(C1017) R^(D4) R^(D225) L_(C1125) R^(D9) R^(D225) L_(C802) R^(D226) R^(D226) L_(C910) R^(D1) R^(D226) L_(C1018) R^(D4) R^(D226) L_(C1126) R^(D9) R^(D226) L_(C803) R^(D227) R^(D227) L_(C911) R^(D1) R^(D227) L_(C1019) R^(D4) R^(D227) L_(C1127) R^(D9) R^(D227) L_(C804) R^(D228) R^(D228) L_(C912) R^(D1) R^(D228) L_(C1020) R^(D4) R^(D228) L_(C1128) R^(D9) R^(D228) L_(C805) R^(D229) R^(D229) L_(C913) R^(D1) R^(D229) L_(C1021) R^(D4) R^(D229) L_(C1129) R^(D9) R^(D229) L_(C806) R^(D230) R^(D230) L_(C914) R^(D1) R^(D230) L_(C1022) R^(D4) R^(D230) L_(C1130) R^(D9) R^(D230) L_(C807) R^(D231) R^(D231) L_(C915) R^(D1) R^(D231) L_(C1023) R^(D4) R^(D231) L_(C1131) R^(D9) R^(D231) L_(C808) R^(D232) R^(D232) L_(C916) R^(D1) R^(D232) L_(C1024) R^(D4) R^(D232) L_(C1132) R^(D9) R^(D232) L_(C809) R^(D233) R^(D233) L_(C917) R^(D1) R^(D233) L_(C1025) R^(D4) R^(D233) L_(C1133) R^(D9) R^(D233) L_(C810) R^(D234) R^(D234) L_(C918) R^(D1) R^(D234) L_(C1026) R^(D4) R^(D234) L_(C1134) R^(D9) R^(D234) L_(C811) R^(D235) R^(D235) L_(C919) R^(D1) R^(D235) L_(C1027) R^(D4) R^(D235) L_(C1135) R^(D9) R^(D235) L_(C812) R^(D236) R^(D236) L_(C920) R^(D1) R^(D236) L_(C1028) R^(D4) R^(D236) L_(C1136) R^(D9) R^(D236) L_(C813) R^(D237) R^(D237) L_(C921) R^(D1) R^(D237) L_(C1029) R^(D4) R^(D237) L_(C1137) R^(D9) R^(D237) L_(C814) R^(D238) R^(D238) L_(C922) R^(D1) R^(D238) L_(C1030) R^(D4) R^(D238) L_(C1138) R^(D9) R^(D238) L_(C815) R^(D239) R^(D239) L_(C923) R^(D1) R^(D239) L_(C1031) R^(D4) R^(D239) L_(C1139) R^(D9) R^(D239) L_(C816) R^(D240) R^(D240) L_(C924) R^(D1) R^(D240) L_(C1032) R^(D4) R^(D240) L_(C1140) R^(D9) R^(D240) L_(C817) R^(D241) R^(D241) L_(C925) R^(D1) R^(D241) L_(C1033) R^(D4) R^(D241) L_(C1141) R^(D9) R^(D241) L_(C818) R^(D242) R^(D242) L_(C926) R^(D1) R^(D242) L_(C1034) R^(D4) R^(D242) L_(C1142) R^(D9) R^(D242) L_(C819) R^(D243) R^(D243) L_(C927) R^(D1) R^(D243) L_(C1035) R^(D4) R^(D243) L_(C1143) R^(D9) R^(D243) L_(C820) R^(D244) R^(D244) L_(C928) R^(D1) R^(D244) L_(C1036) R^(D4) R^(D244) L_(C1144) R^(D9) R^(D244) L_(C821) R^(D245) R^(D245) L_(C929) R^(D1) R^(D245) L_(C1037) R^(D4) R^(D245) L_(C1145) R^(D9) R^(D245) L_(C822) R^(D246) R^(D246) L_(C930) R^(D1) R^(D246) L_(C1038) R^(D4) R^(D246) L_(C1146) R^(D9) R^(D246) L_(C823) R^(D17) R^(D193) L_(C931) R^(D50) R^(D193) L_(C1039) R^(D145) R^(D193) L_(C1147) R^(D168) R^(D193) L_(C824) R^(D17) R^(D194) L_(C932) R^(D50) R^(D194) L_(C1040) R^(D145) R^(D194) L_(C1148) R^(D168) R^(D194) L_(C825) R^(D17) R^(D195) L_(C933) R^(D50) R^(D195) L_(C1041) R^(D145) R^(D195) L_(C1149) R^(D168) R^(D195) L_(C826) R^(D17) R^(D196) L_(C934) R^(D50) R^(D196) L_(C1042) R^(D145) R^(D196) L_(C1150) R^(D168) R^(D196) L_(C827) R^(D17) R^(D197) L_(C935) R^(D50) R^(D197) L_(C1043) R^(D145) R^(D197) L_(C1151) R^(D168) R^(D197) L_(C828) R^(D17) R^(D198) L_(C936) R^(D50) R^(D198) L_(C1044) R^(D145) R^(D198) L_(C1152) R^(D168) R^(D198) L_(C829) R^(D17) R^(D199) L_(C937) R^(D50) R^(D199) L_(C1045) R^(D145) R^(D199) L_(C1153) R^(D168) R^(D199) L_(C830) R^(D17) R^(D200) L_(C938) R^(D50) R^(D200) L_(C1046) R^(D145) R^(D200) L_(C1154) R^(D168) R^(D200) L_(C831) R^(D17) R^(D201) L_(C939) R^(D50) R^(D201) L_(C1047) R^(D145) R^(D201) L_(C1155) R^(D168) R^(D201) L_(C832) R^(D17) R^(D202) L_(C940) R^(D50) R^(D202) L_(C1048) R^(D145) R^(D202) L_(C1156) R^(D168) R^(D202) L_(C833) R^(D17) R^(D203) L_(C941) R^(D50) R^(D203) L_(C1049) R^(D145) R^(D203) L_(C1157) R^(D168) R^(D203) L_(C834) R^(D17) R^(D204) L_(C942) R^(D50) R^(D204) L_(C1050) R^(D145) R^(D204) L_(C1158) R^(D168) R^(D204) L_(C835) R^(D17) R^(D205) L_(C943) R^(D50) R^(D205) L_(C1051) R^(D145) R^(D205) L_(C1159) R^(D168) R^(D205) L_(C836) R^(D17) R^(D206) L_(C944) R^(D50) R^(D206) L_(C1052) R^(D145) R^(D206) L_(C1160) R^(D168) R^(D206) L_(C837) R^(D17) R^(D207) L_(C945) R^(D50) R^(D207) L_(C1053) R^(D145) R^(D207) L_(C1161) R^(D168) R^(D207) L_(C838) R^(D17) R^(D208) L_(C946) R^(D50) R^(D208) L_(C1054) R^(D145) R^(D208) L_(C1162) R^(D168) R^(D208) L_(C839) R^(D17) R^(D209) L_(C947) R^(D50) R^(D209) L_(C1055) R^(D145) R^(D209) L_(C1163) R^(D168) R^(D209) L_(C840) R^(D17) R^(D210) L_(C948) R^(D50) R^(D210) L_(C1056) R^(D145) R^(D210) L_(C1164) R^(D168) R^(D210) L_(C841) R^(D17) R^(D211) L_(C949) R^(D50) R^(D211) L_(C1057) R^(D145) R^(D211) L_(C1165) R^(D168) R^(D211) L_(C842) R^(D17) R^(D212) L_(C950) R^(D50) R^(D212) L_(C1058) R^(D145) R^(D212) L_(C1166) R^(D168) R^(D212) L_(C843) R^(D17) R^(D213) L_(C951) R^(D50) R^(D213) L_(C1059) R^(D145) R^(D213) L_(C1167) R^(D168) R^(D213) L_(C844) R^(D17) R^(D214) L_(C952) R^(D50) R^(D214) L_(C1060) R^(D145) R^(D214) L_(C1168) R^(D168) R^(D214) L_(C845) R^(D17) R^(D215) L_(C953) R^(D50) R^(D215) L_(C1061) R^(D145) R^(D215) L_(C1169) R^(D168) R^(D215) L_(C846) R^(D17) R^(D216) L_(C954) R^(D50) R^(D216) L_(C1062) R^(D145) R^(D216) L_(C1170) R^(D168) R^(D216) L_(C847) R^(D17) R^(D217) L_(C955) R^(D50) R^(D217) L_(C1063) R^(D145) R^(D217) L_(C1171) R^(D168) R^(D217) L_(C848) R^(D17) R^(D218) L_(C956) R^(D50) R^(D218) L_(C1064) R^(D145) R^(D218) L_(C1172) R^(D168) R^(D218) L_(C849) R^(D17) R^(D219) L_(C957) R^(D50) R^(D219) L_(C1065) R^(D145) R^(D219) L_(C1173) R^(D168) R^(D219) L_(C850) R^(D17) R^(D220) L_(C958) R^(D50) R^(D220) L_(C1066) R^(D145) R^(D220) L_(C1174) R^(D168) R^(D220) L_(C851) R^(D17) R^(D221) L_(C959) R^(D50) R^(D221) L_(C1067) R^(D145) R^(D221) L_(C1175) R^(D168) R^(D221) L_(C852) R^(D17) R^(D222) L_(C960) R^(D50) R^(D222) L_(C1068) R^(D145) R^(D222) L_(C1176) R^(D168) R^(D222) L_(C853) R^(D17) R^(D223) L_(C961) R^(D50) R^(D223) L_(C1069) R^(D145) R^(D223) L_(C1177) R^(D168) R^(D223) L_(C854) R^(D17) R^(D224) L_(C962) R^(D50) R^(D224) L_(C1070) R^(D145) R^(D224) L_(C1178) R^(D168) R^(D224) L_(C855) R^(D17) R^(D225) L_(C963) R^(D50) R^(D225) L_(C1071) R^(D145) R^(D225) L_(C1179) R^(D168) R^(D225) L_(C856) R^(D17) R^(D226) L_(C964) R^(D50) R^(D226) L_(C1072) R^(D145) R^(D226) L_(C1180) R^(D168) R^(D226) L_(C857) R^(D17) R^(D227) L_(C965) R^(D50) R^(D227) L_(C1073) R^(D145) R^(D227) L_(C1181) R^(D168) R^(D227) L_(C858) R^(D17) R^(D228) L_(C966) R^(D50) R^(D228) L_(C1074) R^(D145) R^(D228) L_(C1182) R^(D168) R^(D228) L_(C859) R^(D17) R^(D229) L_(C967) R^(D50) R^(D229) L_(C1075) R^(D145) R^(D229) L_(C1183) R^(D168) R^(D229) L_(C860) R^(D17) R^(D230) L_(C968) R^(D50) R^(D230) L_(C1076) R^(D145) R^(D230) L_(C1184) R^(D168) R^(D230) L_(C861) R^(D17) R^(D231) L_(C969) R^(D50) R^(D231) L_(C1077) R^(D145) R^(D231) L_(C1185) R^(D168) R^(D231) L_(C862) R^(D17) R^(D232) L_(C970) R^(D50) R^(D232) L_(C1078) R^(D145) R^(D232) L_(C1186) R^(D168) R^(D232) L_(C863) R^(D17) R^(D233) L_(C971) R^(D50) R^(D233) L_(C1079) R^(D145) R^(D233) L_(C1187) R^(D168) R^(D233) L_(C864) R^(D17) R^(D234) L_(C972) R^(D50) R^(D234) L_(C1080) R^(D145) R^(D234) L_(C1188) R^(D168) R^(D234) L_(C865) R^(D17) R^(D235) L_(C973) R^(D50) R^(D235) L_(C1081) R^(D145) R^(D235) L_(C1189) R^(D168) R^(D235) L_(C866) R^(D17) R^(D236) L_(C974) R^(D50) R^(D236) L_(C1082) R^(D145) R^(D236) L_(C1190) R^(D168) R^(D236) L_(C867) R^(D17) R^(D237) L_(C975) R^(D50) R^(D237) L_(C1083) R^(D145) R^(D237) L_(C1191) R^(D168) R^(D237) L_(C868) R^(D17) R^(D238) L_(C976) R^(D50) R^(D238) L_(C1084) R^(D145) R^(D238) L_(C1192) R^(D168) R^(D238) L_(C869) R^(D17) R^(D239) L_(C977) R^(D50) R^(D239) L_(C1085) R^(D145) R^(D239) L_(C1193) R^(D168) R^(D239) L_(C870) R^(D17) R^(D240) L_(C978) R^(D50) R^(D240) L_(C1086) R^(D145) R^(D240) L_(C1194) R^(D168) R^(D240) L_(C871) R^(D17) R^(D241) L_(C979) R^(D50) R^(D241) L_(C1087) R^(D145) R^(D241) L_(C1195) R^(D168) R^(D241) L_(C872) R^(D17) R^(D242) L_(C980) R^(D50) R^(D242) L_(C1088) R^(D145) R^(D242) L_(C1196) R^(D168) R^(D242) L_(C873) R^(D17) R^(D243) L_(C981) R^(D50) R^(D243) L_(C1089) R^(D145) R^(D243) L_(C1197) R^(D168) R^(D243) L_(C874) R^(D17) R^(D244) L_(C982) R^(D50) R^(D244) L_(C1090) R^(D145) R^(D244) L_(C1198) R^(D168) R^(D244) L_(C875) R^(D17) R^(D245) L_(C983) R^(D50) R^(D245) L_(C1091) R^(D145) R^(D245) L_(C1199) R^(D168) R^(D245) L_(C876) R^(D17) R^(D246) L_(C984) R^(D50) R^(D246) L_(C1092) R^(D145) R^(D246) L_(C1200) R^(D168) R^(D246) L_(C1201) R^(D10) R^(D193) L_(C1255) R^(D55) R^(D193) L_(C1309) R^(D37) R^(D193) L_(C1363) R^(D143) R^(D193) L_(C1202) R^(D10) R^(D194) L_(C1256) R^(D55) R^(D194) L_(C1310) R^(D37) R^(D194) L_(C1364) R^(D143) R^(D194) L_(C1203) R^(D10) R^(D195) L_(C1257) R^(D55) R^(D195) L_(C1311) R^(D37) R^(D195) L_(C1365) R^(D143) R^(D195) L_(C1204) R^(D10) R^(D196) L_(C1258) R^(D55) R^(D196) L_(C1312) R^(D37) R^(D196) L_(C1366) R^(D143) R^(D196) L_(C1205) R^(D10) R^(D197) L_(C1259) R^(D55) R^(D197) L_(C1313) R^(D37) R^(D197) L_(C1367) R^(D143) R^(D197) L_(C1206) R^(D10) R^(D198) L_(C1260) R^(D55) R^(D198) L_(C1314) R^(D37) R^(D198) L_(C1368) R^(D143) R^(D198) L_(C1207) R^(D10) R^(D199) L_(C1261) R^(D55) R^(D199) L_(C1315) R^(D37) R^(D199) L_(C1369) R^(D143) R^(D199) L_(C1208) R^(D10) R^(D200) L_(C1262) R^(D55) R^(D200) L_(C1316) R^(D37) R^(D200) L_(C1370) R^(D143) R^(D200) L_(C1209) R^(D10) R^(D201) L_(C1263) R^(D55) R^(D201) L_(C1317) R^(D37) R^(D201) L_(C1371) R^(D143) R^(D201) L_(C1210) R^(D10) R^(D202) L_(C1264) R^(D55) R^(D202) L_(C1318) R^(D37) R^(D202) L_(C1372) R^(D143) R^(D202) L_(C1211) R^(D10) R^(D203) L_(C1265) R^(D55) R^(D203) L_(C1319) R^(D37) R^(D203) L_(C1373) R^(D143) R^(D203) L_(C1212) R^(D10) R^(D204) L_(C1266) R^(D55) R^(D204) L_(C1320) R^(D37) R^(D204) L_(C1374) R^(D143) R^(D204) L_(C1213) R^(D10) R^(D205) L_(C1267) R^(D55) R^(D205) L_(C1321) R^(D37) R^(D205) L_(C1375) R^(D143) R^(D205) L_(C1214) R^(D10) R^(D206) L_(C1268) R^(D55) R^(D206) L_(C1322) R^(D37) R^(D206) L_(C1376) R^(D143) R^(D206) L_(C1215) R^(D10) R^(D207) L_(C1269) R^(D55) R^(D207) L_(C1323) R^(D37) R^(D207) L_(C1377) R^(D143) R^(D207) L_(C1216) R^(D10) R^(D208) L_(C1270) R^(D55) R^(D208) L_(C1324) R^(D37) R^(D208) L_(C1378) R^(D143) R^(D208) L_(C1217) R^(D10) R^(D209) L_(C1271) R^(D55) R^(D209) L_(C1325) R^(D37) R^(D209) L_(C1379) R^(D143) R^(D209) L_(C1218) R^(D10) R^(D210) L_(C1272) R^(D55) R^(D210) L_(C1326) R^(D37) R^(D210) L_(C1380) R^(D143) R^(D210) L_(C1219) R^(D10) R^(D211) L_(C1273) R^(D55) R^(D211) L_(C1327) R^(D37) R^(D211) L_(C1381) R^(D143) R^(D211) L_(C1220) R^(D10) R^(D212) L_(C1274) R^(D55) R^(D212) L_(C1328) R^(D37) R^(D212) L_(C1382) R^(D143) R^(D212) L_(C1221) R^(D10) R^(D213) L_(C1275) R^(D55) R^(D213) L_(C1329) R^(D37) R^(D213) L_(C1383) R^(D143) R^(D213) L_(C1222) R^(D10) R^(D214) L_(C1276) R^(D55) R^(D214) L_(C1330) R^(D37) R^(D214) L_(C1384) R^(D143) R^(D214) L_(C1223) R^(D10) R^(D215) L_(C1277) R^(D55) R^(D215) L_(C1331) R^(D37) R^(D215) L_(C1385) R^(D143) R^(D215) L_(C1224) R^(D10) R^(D216) L_(C1278) R^(D55) R^(D216) L_(C1332) R^(D37) R^(D216) L_(C1386) R^(D143) R^(D216) L_(C1225) R^(D10) R^(D217) L_(C1279) R^(D55) R^(D217) L_(C1333) R^(D37) R^(D217) L_(C1387) R^(D143) R^(D217) L_(C1226) R^(D10) R^(D218) L_(C1280) R^(D55) R^(D218) L_(C1334) R^(D37) R^(D218) L_(C1388) R^(D143) R^(D218) L_(C1227) R^(D10) R^(D219) L_(C1281) R^(D55) R^(D219) L_(C1335) R^(D37) R^(D219) L_(C1389) R^(D143) R^(D219) L_(C1228) R^(D10) R^(D220) L_(C1282) R^(D55) R^(D220) L_(C1336) R^(D37) R^(D220) L_(C1390) R^(D143) R^(D220) L_(C1229) R^(D10) R^(D221) L_(C1283) R^(D55) R^(D221) L_(C1337) R^(D37) R^(D221) L_(C1391) R^(D143) R^(D221) L_(C1230) R^(D10) R^(D222) L_(C1284) R^(D55) R^(D222) L_(C1338) R^(D37) R^(D222) L_(C1392) R^(D143) R^(D222) L_(C1231) R^(D10) R^(D223) L_(C1285) R^(D55) R^(D223) L_(C1339) R^(D37) R^(D223) L_(C1393) R^(D143) R^(D223) L_(C1232) R^(D10) R^(D224) L_(C1286) R^(D55) R^(D224) L_(C1340) R^(D37) R^(D224) L_(C1394) R^(D143) R^(D224) L_(C1233) R^(D10) R^(D225) L_(C1287) R^(D55) R^(D225) L_(C1341) R^(D37) R^(D225) L_(C1395) R^(D143) R^(D225) L_(C1234) R^(D10) R^(D226) L_(C1288) R^(D55) R^(D226) L_(C1342) R^(D37) R^(D226) L_(C1396) R^(D143) R^(D226) L_(C1235) R^(D10) R^(D227) L_(C1289) R^(D55) R^(D227) L_(C1343) R^(D37) R^(D227) L_(C1397) R^(D143) R^(D227) L_(C1236) R^(D10) R^(D228) L_(C1290) R^(D55) R^(D228) L_(C1344) R^(D37) R^(D228) L_(C1398) R^(D143) R^(D228) L_(C1237) R^(D10) R^(D229) L_(C1291) R^(D55) R^(D229) L_(C1345) R^(D37) R^(D229) L_(C1399) R^(D143) R^(D229) L_(C1238) R^(D10) R^(D230) L_(C1292) R^(D55) R^(D230) L_(C1346) R^(D37) R^(D230) L_(C1400) R^(D143) R^(D230) L_(C1239) R^(D10) R^(D231) L_(C1293) R^(D55) R^(D231) L_(C1347) R^(D37) R^(D231) L_(C1401) R^(D143) R^(D231) L_(C1240) R^(D10) R^(D232) L_(C1294) R^(D55) R^(D232) L_(C1348) R^(D37) R^(D232) L_(C1402) R^(D143) R^(D232) L_(C1241) R^(D10) R^(D233) L_(C1295) R^(D55) R^(D233) L_(C1349) R^(D37) R^(D233) L_(C1403) R^(D143) R^(D233) L_(C1242) R^(D10) R^(D234) L_(C1296) R^(D55) R^(D234) L_(C1350) R^(D37) R^(D234) L_(C1404) R^(D143) R^(D234) L_(C1243) R^(D10) R^(D235) L_(C1297) R^(D55) R^(D235) L_(C1351) R^(D37) R^(D235) L_(C1405) R^(D143) R^(D235) L_(C1244) R^(D10) R^(D236) L_(C1298) R^(D55) R^(D236) L_(C1352) R^(D37) R^(D236) L_(C1406) R^(D143) R^(D236) L_(C1245) R^(D10) R^(D237) L_(C1299) R^(D55) R^(D237) L_(C1353) R^(D37) R^(D237) L_(C1407) R^(D143) R^(D237) L_(C1246) R^(D10) R^(D238) L_(C1300) R^(D55) R^(D238) L_(C1354) R^(D37) R^(D238) L_(C1408) R^(D143) R^(D238) L_(C1247) R^(D10) R^(D239) L_(C1301) R^(D55) R^(D239) L_(C1355) R^(D37) R^(D239) L_(C1409) R^(D143) R^(D239) L_(C1248) R^(D10) R^(D240) L_(C1302) R^(D55) R^(D240) L_(C1356) R^(D37) R^(D240) L_(C1410) R^(D143) R^(D240) L_(C1249) R^(D10) R^(D241) L_(C1303) R^(D55) R^(D241) L_(C1357) R^(D37) R^(D241) L_(C1411) R^(D143) R^(D241) L_(C1250) R^(D10) R^(D242) L_(C1304) R^(D55) R^(D242) L_(C1358) R^(D37) R^(D242) L_(C1412) R^(D143) R^(D242) L_(C1251) R^(D10) R^(D243) L_(C1305) R^(D55) R^(D243) L_(C1359) R^(D37) R^(D243) L_(C1413) R^(D143) R^(D243) L_(C1252) R^(D10) R^(D244) L_(C1306) R^(D55) R^(D244) L_(C1360) R^(D37) R^(D244) L_(C1414) R^(D143) R^(D244) L_(C1253) R^(D10) R^(D245) L_(C1307) R^(D55) R^(D245) L_(C1361) R^(D37) R^(D245) L_(C1415) R^(D143) R^(D245) L_(C1254) R^(D10) R^(D246) L_(C1308) R^(D55) R^(D246) L_(C1362) R^(D37) R^(D246) L_(C1416) R^(D143) R^(D246);

wherein R^(D1) to R^(D246) have the following structures:


15. The compound of claim 1, wherein the compound is selected from the group consisting of:


16. The compound of claim 11 wherein the compound has a structure of Formula II

wherein: M¹ is Pd or Pt; moieties E and F are each independently a monocyclic or polycyclic ring structure comprising 5-membered and/or 6-membered carbocyclic or heterocyclic rings; Z¹ and Z² are each independently C or N; K¹ and K² are each independently selected from the group consisting of a direct bond, O, and S, wherein at least one of K, K, and K² is a direct bond; L¹, L², and L³ are each independently selected from the group consisting of a single bond, absent a bond, O, Se, S, SO, SO₂, C═CR′R″, C═NR′, CR′R″, SiR′R″, BR′, P(O)R′, and NR′, wherein at least one of L¹ and L² is present; X^(3′) and X^(4′) are each independently C or N; R^(E) and R^(F) each independently represent zero, mono, or up to a maximum allowed substitution to its associated ring; each of R′, R″, R^(E), and R^(F) is independently a hydrogen or a substituent selected from the group consisting of deuterium, fluorine, alkyl, cycloalkyl, heteroalkyl, alkoxy, aryloxy, amino, silyl, boryl, alkenyl, cycloalkenyl, heteroalkenyl, aryl, heteroaryl, nitrile, isonitrile, sulfanyl, and combinations thereof; and two of R, R′, R″, R^(A), R^(E), and R^(F), can be joined or fused together to form a ring.
 17. An organic light emitting device (OLED) comprising: an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a compound comprising a first ligand L_(A) of Formula I,

wherein ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring; wherein K is selected from the group consisting of a direct bond, O, S, NR′, CR′R″, and SiR′R″; wherein two adjacent ones of X¹ to X⁴ are C and are fused to form a structure of Formula II,

wherein the dashed lines indicate direct bonds to ring B; wherein each of X¹ to X¹² independently represents C, CR or N, and each R can be same or different; wherein X is selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, Ge′RR″, SnR′R″, BR′, PR′, SbR′, and BiR′; wherein R^(A) represent mono to the maximum allowable substitution, or no substitution; wherein each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, gennyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, selenyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein L_(A) is coordinated to a metal M through the indicated dashed lines; wherein the metal M has an atomic mass greater than 40; wherein the metal M can be coordinated to other ligands; wherein L_(A) may be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and wherein any two adjacent R, R′, R″, and R^(A) can be joined or fused to form a ring, with the proviso that that (1) when X is CR′R″, X⁵ is CR; and (2) when X is O, S, Se, or NR′, at least one of the following is true: (a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand; (b) at least one R comprises an electron withdrawing group; (c) at least two R^(A) is not hydrogen or deuterium; or (d) at least one R is selected from the group consisting of the structures of LIST 1 as defined herein.
 18. The OLED of claim 17, wherein the organic layer further comprises a host, wherein host comprises at least one chemical moiety selected from the group consisting of triphenylene, carbazole, indolocarbazole, dibenzothiophene, dibenzofuran, dibenzoselenophene, 5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene, aza-triphenylene, aza-carbazole, aza-indolocarbazole, aza-dibenzothiophene, aza-dibenzofuran, aza-dibenzoselenophene, and aza-(5,9-dioxa-13b-boranaphtho[3,2,1-de]anthracene).
 19. The OLED of claim 18, wherein the host is selected from the group consisting of the HOST Group defined herein.
 20. A consumer product comprising an organic light-emitting device (OLED) comprising: an anode; a cathode; and an organic layer disposed between the anode and the cathode, wherein the organic layer comprises a compound comprising a first ligand L_(A) of Formula I,

wherein ring A is a 5-membered or 6-membered carbocyclic or heterocyclic ring; wherein K is selected from the group consisting of a direct bond, O, S, NR′, CR′R″, and SiR′R″; wherein two adjacent ones of X¹ to X⁴ are C and are fused to form a structure of Formula II,

wherein the dashed lines indicate direct bonds to ring B; wherein each of X¹ to X¹² independently represents C, CR or N, and each R can be same or different; wherein X is selected from the group consisting of O, S, Se, NR′, CR′R″, SiR′R″, Ge′RR″, SnR′R″, BR′, PR′, SbR′, and BiR′; wherein R^(A) represent mono to the maximum allowable substitution, or no substitution; wherein each R, R′, R″, and R^(A) is independently a hydrogen or a substituent selected from the group consisting of deuterium, halogen, alkyl, cycloalkyl, heteroalkyl, heterocycloalkyl, boryl, arylalkyl, alkoxy, aryloxy, amino, silyl, germyl, alkenyl, cycloalkenyl, heteroalkenyl, alkynyl, aryl, heteroaryl, acyl, carboxylic acid, ether, ester, nitrile, isonitrile, sulfanyl, selenyl, sulfinyl, sulfonyl, phosphino, and combinations thereof; wherein L_(A) is coordinated to a metal M through the indicated dashed lines; wherein the metal M has an atomic mass greater than 40; wherein the metal M can be coordinated to other ligands; wherein L_(A) may be joined with other ligands to comprise a tridentate, tetradentate, pentadentate, and hexadentate ligand; and wherein any two adjacent R, R′, R″, and R^(A) can be joined or fused to form a ring, with the proviso that that (1) when X is CR′R″, X⁵ is CR; and (2) when X is O, S, Se, or NR′, at least one of the following is true: (a) the metal M is further coordinated to at least one substituted or unsubstituted acetylacetonate ligand; (b) at least one R comprises an electron withdrawing group; (c) at least two R^(A) is not hydrogen or deuterium; or (d) at least one R is selected from the group consisting of the structures of LIST 1 as defined herein. 